Tender for Health And Family Welfare Department - NTID 23264755
Health And Family Welfare Department
Vadodara, Gujarat, India
NTID 23264755
- Opening Date : Sat 5th December, 2020
- Closing Date : Mon 21st December, 2020
- ₹ 0.00
- NTID 23264755
supply of surgical items (1 to 4829) -part 8 (item no 2451 to 2800) - incisde drape made up of polyester film with an acrylic adhesive that contains a, complex of iodoform(n- vinyl 2 pyrrolidine) with a iodine concentration of 0.092, mg iodine/cm2. film should be breathable and conformable to skin, compatible with, povidone and chg skin preps. iodine from the drape should be present in the, deepest skin layers (1000 microns depth) where hair folices exist apart from killing, microbes on skin layer. incise area : 34 cm x 35 cm, incisde drape made up of polyester film with an acrylic adhesive that contains a, complex of iodoform(n- vinyl 2 pyrrolidine) with a iodine concentration of 0.092, mg iodine/cm2. film should be breathable and conformable to skin, compatible with, povidone and chg skin preps. iodine from the drape should be present in the, deepest skin layers (1000 microns depth) where hair folices exist apart from killing, microbes on skin layer.incise area : 56cm x 45cm, incisde drape made up of polyester film with an acrylic adhesive that contains a, complex of iodoform(n- vinyl 2 pyrrolidine) with a iodine concentration of 0.092, mg iodine/cm2. film should be breathable and conformable to skin, compatible with, povidone and chg skin preps. iodine from the drape should be present in the, deepest skin layers (1000 microns depth) where hair folices exist apart from killing, microbes on skin layer. incise area : 10cm x 20cm, incise drape made up of polyester film with an acrylic adhesive that contains a, complex of iodoform(n- vinyl 2 pyrrolidine) with a iodine concentration of 0.092, mg iodine/cm2. film should be breathable and conformable to skin, compatible with, povidone and chg skin preps. iodine from the drape should be present in the, deepest skin layers (1000 microns depth) where hair folices exist apart from killing, microbes on skin layer 30cm x 30cm, incise drape which is antimicrobial, strong, conformable and breathable iodophor, impregnated polyester film coated with hypoallergenic adhesive for superior, adhesion. contains a framed delivery system for one-person drape application,, designed specifically for minimally invasive surgical procedure.compatible with, povidine iodine & chg preps.latex free.26cm x 20cm, incisde drape made up of polyester film with an acrylic adhesive that contains a, complex of iodoform(n- vinyl 2 pyrrolidine) with a iodine concentration of 0.092, mg iodine/cm2. film should be breathable and conformable to skin, compatible with, povidone and chg skin preps. iodine from the drape should be present in the, deepest skin layers (1000 microns depth) where hair folices exist apart from killing, microbes on skin layer. 56cm x 60cm, waterless alcohol based handrub for hand hygiene, uniquely formulated (2-, propanol – 45% w/w, 1- propanol – 30%w/w, ethyl – hexadecyl – dimethyl, ammonium sulphate – 0.2 w/w, with emollient & moisturizer to be used with a twin, purpose wall mount/bed-side dispenser. broad spectrum antimicrobial, bactericidal, sporicidal, fungicidal, virucidal)., waterless chg and alcohol based handrub for hand hygiene, uniquely formulated, chlorhexidine gluconate ip 2.5% v/v (equivalent to 0.5% w/v chlorhexidine, gluconate) and ethanol ip 70% v/v with moisturizer and emollients. broad, spectrum antimicrobial., chg is found to bind better to the stratum corneum (or the outermost layer of skin,, acting as a barrier to keep bacteria out and hold moisture in) providing for a longer, duration of anti-microbial action. fully documented compliance with the following, supported by govt certified labs or third party labs certification: iso 10993 part, 10,2010 : test for irritation and skin sensitization,en1040-2005 : bactericidal and, en 1275-2005 : yeasticidal,usp-36 disinfectant and antiseptics 1072:2013, fungicidal and sporicidal, hcipt (human cumulative irritancy patch test., appraised efficacy in compliance with astm test method # 2315, recommended, for use in medical applications - polyurethanes can outperform many other materials, in flexibility, tear resistance and abrasion resistance., open cell foam – common benefits of this material is they are soft and breathable,, more flexible and returns easily to its original state after compressing. high density, of 28.8 to 35.2 kg/m3 – higher resilience and commonly withstands high usage, surgical skin prepping antiseptic solution, uniquely formulated - povidone-iodine, ip 10% w/v (equivalent to 1% w/v available iodine) water ip qs. broad spectrum, antimicrobial (bactericidal, sporicidal, fungicidal, virucidal)., chlorhexidine gluconate scrub solution 4% w/v (equivalent to 20% v/v) - broad, spectrum (bactericidal, fungicidal, virucidal and sporicidal) antimicrobial solution, for surgical scrubbing and pre-operative patient showering, in a translucent bottle, with volume calibration,500ml, non woven 3 layered sterile, lightweight, breathable and low linting surgical, disposable gown with alocohol repellant & anti static fabric. made of 43 gsm, fabric with alcohol repellancy (aatcc193-2012) level 8. low linting, indivually, sterile packed with 2 absorbent paper towels. size xl- 137 cm (l) * 160 cm(w), surgical hand and skin scrubbing antiseptic solution, uniquely formulated -, povidone-iodine ip 7.5% w/v (equivalent to 0.75% w/v available iodine) water ip, qs. broad spectrum antimicrobial (bactericidal, sporicidal, fungicidal, virucidal)., high barrier disposable surgical drapes made of reinforced spunbond-film composite, which is a blue laminate of polypropylene nonwoven and a polyethylene film, offering absorbency yet imperviousness to fluid strike-through across the entire, drape material. it should be low-linting, non-breathable with an adhesive area,, wherever incorporated, containing hypoallergenic acrylate type adhesive covered, with a silicone coated paper liner and should also comply with the requirements of, iso 13485:2003,a basic surgical pack with the above features should contain 2nos, of cautery bags(size 30cm x 35cm), 1no of operation tape(size 10cm x 55cm), 4nos, of hand towels(23.5cm x 38cm), 2nos of adhesive towel drape(size 91.5cm x, 100cm), 1no of adhesive medium drape sheet(size 183cm x 183cm), 1no of adhesive, large drape sheet(size 150cm x 250cm), 1no of instrument table cover(150cm x, 200cm), 1no of large instrument table cover(size 183cm x 240cm), broad spectrum virucidal, bactericidal and fungicidal waterless alcohol based handrub, for hand hygiene, containing 75% v/v iso-propyl alcohol, moisturizer and, emollients with a wall-mounting/bed-side stand,500ml, waterless alcohol based handrub for hand hygiene, uniquely formulated (2-, propanol – 45% w/w, 1- propanol – 30%w/w, ethyl – hexadecyl – dimethyl, ammonium sulphate – 0.2 w/w, with emollient & moisturizer. broad spectrum, antimicrobial (bactericidal, sporicidal, fungicidal, virucidal),100ml, chlorhexidine gluconate scrub solution 2% w/v (equivalent to 10% v/v) – broad spectrum, chlorhexidine gluconate scrub solution 2% w/v (equivalent to 10% v/v) – broad speactsru, product must be made of low-linting, nonwoven, absorbent fabric laminated to a, plastic film. must be resistant to fluid strikethrough. must be absorbent throughout, the entire drape, this eliminating the need to define a “critical zone”. must meet, flammability class 1 (cfr title 16 part 1610). components include: cautery bags, (30cm x 35cm) - 4 nos, operation tapes (10cm x 55cm) - 3 no, hand towels -, (23.5cm x 38cm) - 4 nos, adhesive towel drapes - (91.5cm x 100cm) - 4 nos,, adhesive drape sheet (m) - (183cm x 183cm) - 1 no, adhesive drape sheet (l) -, (150cm x 250cm) - 1 no, instrument table cover - (150cm x 200cm) - 1 no,, instrument table cover (l) - (183cm x 240cm) - 1 no, bilateral split sheet -, (183cm x 200cm) - 1 no, triangular drape sheets - (91.5cm x 91.5cm x 129cm) - 2, nos, surgical skin prepping antiseptic solution, uniquely formulated - povidone-iodine, ip 5% w/v (equivalent to 0.5% w/v available iodine) water ip qs. broad spectrum, microbicidal solution (bactericidal, sporicidal, fungicidal)., waterless chg and alcohol based handrub for hand hygiene, uniquely formulated, chlorhexidine gluconate ip 2.5% v/v (equivalent to 0.5% w/v chlorhexidine, gluconate) and ethanol ip 70% v/v with moisturizer and emollients. broad, spectrum antimicrobial,100ml, non woven 3 layered sterile, lightweight, breathable and low linting surgical, disposable gown with alocohol repellant & anti static fabric. made of 43 gsm, fabric with alcohol repellancy (aatcc193-2012) level 8. low linting, indivually, sterile packed with 2 absorbent paper towels. size l - 132 cm (l) * 150 cm (w), a transparent and a clear drape that should provide a reliable barrier to bacteria on, the skin. must come equipped with a reliable and secure adhesive and should be, available at 10 units per pack. length must be 23 inch and width must be 17 inches., must be iso certified, chlorhexidine gluconate scrub solution 4% w/v (equivalent to 20% v/v) - broad, spectrum (bactericidal, fungicidal, virucidal and sporicidal) antimicrobial solution, for surgical scrubbing and pre-operative patient showering, in a translucent bottle, with volume calibration,100ml, non woven 4 layered sterile, lightweight, breathable and low linting surgical, disposable gown with outer and inner layer made of strong and spun bond, repellent fabric, and two middle layers offering fluid control and bacterial barrier., ce certified, tvyek outer packaging., waterless alcohol based handrub for hand hygiene, uniquely formulated (2-, propanol – 45% w/w, 1- propanol – 30%w/w, ethyl – hexadecyl – dimethyl, ammonium sulphate – 0.2 w/w, with emollient & moisturizer. broad spectrum, antimicrobial (bactericidal, sporicidal, fungicidal, virucidal),100ml with pump, surgical hand and skin scrubbing antiseptic solution, uniquely formulated -, povidone-iodine ip 7.5% w/v (equivalent to 0.75% w/v available iodine) water ip, qs. broad spectrum antimicrobial (bactericidal, sporicidal, fungicidal,, virucidal),100ml, sterile isolation bag composed of ethyl methyl acrylate (ema) film with polyester, drawstring closure. can be used in sterile field to isolate and contain organs and, body parts for surgical procedures., 20 inches x 20 inches (50 cm x 50 cm), waterless chg and alcohol based handrub for hand hygiene, uniquely formulated, chlorhexidine gluconate ip 2.5% v/v (equivalent to 0.5% w/v chlorhexidine, gluconate) and ethanol ip 70% v/v with moisturizer and emollients. broad, spectrum antimicrobial., waterless foam based chg and alcohol based handrub for hand hygiene, uniquely, formulated - chlorhexidine gluconate ip 2.5% v/v (equivalent to 0.5% w/v, chlorhexidine gluconate) and ethanol ip 70% v/v with moisturizer and emollients, with unique drip resistant dispenser design. broad spectrum antimicrobial,500ml, product must be made of low-linting, nonwoven, absorbent fabric laminated to a, plastic film. must be resistant to fluid strikethrough. must be absorbent throughout, the entire drape, this eliminating the need to define a “critical zone”. must meet, flammability class 1 (cfr title 16 part 1610). components include: adhesive, drape sheet - (228cm x 330cm) - 1 no, transparent, conformable, strike proof, matte finish, and plastic polyethylene split, sheet with u- aperture cut in one end of drape, to isolate (operative area) sterile, field from unclean area. u-aperture coated with a pressure sensitive adhesive lining, for secural., chlorhexidine gluconate scrub solution 2% w/v (equivalent to 10% v/v) – broad, spectrum (bactericidal, fungicidal, virucidal and sporicidal) antimicrobial solution, for skin preparation in a translucent bottle with volume calibration,100ml, fda approved waterless, brushless, scrubless chg & ethanol based surgical hand, antiseptic with moisturizers containing chlorhexidine gluconate 1% w/w and ethyl, alcohol 61% w/w supplied with a foot pump for touchless delivery with 500ml pack, size, high barrier disposable surgical drapes made of reinforced spunbond-film composite, which is a blue laminate of polypropylene nonwoven and a polyethylene film, offering absorbency yet imperviousness to fluid strike-through across the entire, drape material. it should be low-linting, non-breathable with an adhesive area,, wherever incorporated, containing hypoallergenic acrylate type adhesive covered, with a silicone coated paper liner and should also comply with the requirements of, iso 13485:2003, transparent, conformable, strike proof, matte finish, and plastic polyethylene split, sheet with u- aperture cut in one end of drape, to isolate (operative area) sterile, field from unclean area. u-aperture coated with a pressure sensitive adhesive lining, for secural., waterless foam based chg and alcohol based handrub for hand hygiene, uniquely, formulated - chlorhexidine gluconate ip 2.5% v/v (equivalent to 0.5% w/v, chlorhexidine gluconate) and ethanol ip 70% v/v with moisturizer and emollients, with unique drip resistant dispenser design. broad spectrum antimicrobial,50ml, high barrier disposable surgical drapes made of reinforced spunbond-film composite, which is a blue laminate of polypropylene nonwoven and a polyethylene film, offering absorbency yet imperviousness to fluid strike-through across the entire, drape material. it should be low-linting, non-breathable with an adhesive area,, wherever incorporated, containing hypoallergenic acrylate type adhesive covered, with a silicone coated paper liner and should also comply with the requirements of, iso 13485:2003 and iso 9001:2008. the pack with above features should contain, 1no of bilateral knee drape (size 300cm x 370cm)., surgical skin prepping antiseptic solution, uniquely formulated - povidone-iodine, ip 5% w/v (equivalent to 0.5% w/v available iodine) water ip qs. broad spectrum, microbicidal solution (bactericidal, sporicidal, fungicidal),100ml, non woven 3 layered sterile, lightweight, breathable and low linting surgical, disposable gown with alocohol repellant & anti static fabric. made of 43 gsm, fabric with alcohol repellancy (aatcc193-2012) level 8. low linting, indivually, sterile packed with 2 absorbent paper towels., high barrier disposable surgical drapes made of reinforced spunbond-film composite, which is a blue laminate of polypropylene nonwoven and a polyethylene film, offering absorbency yet imperviousness to fluid strike-through across the entire, drape material. it should be low-linting, non-breathable with an adhesive area,, wherever incorporated, containing hypoallergenic acrylate type adhesive covered, with a silicone coated paper liner and should also comply with the requirements of, iso 13485:2003 and iso 9001:2008. a hip drape with above features should, contain 2nos of cautery bags(size 30cm x 35cm), 3no of operation tape(size 10cm x, 55cm), 4nos of hand towels(23.5cm x 38cm), 1no of adhesive split sheet (size, 228cm x 260cm), 1no of hip drape (size 300cm x 353cm), 1no of instrument table, cover(150cm x 200cm), 1no of large instrument table cover(size 183cm x 240cm)., high barrier disposable surgical drapes made of reinforced spunbond-film composite, which is a blue laminate of polypropylene nonwoven and a polyethylene film, offering absorbency yet imperviousness to fluid strike-through across the entire, drape material. it should be low-linting, non-breathable with an adhesive area,, wherever incorporated, containing hypoallergenic acrylate type adhesive covered, with a silicone coated paper liner and should also comply with the requirements of, iso 13485:2003 and iso 9001:2008. the pack with above features should contain, 2nos of cautery bags(size 30cm x 35cm), 3no of operation tape(size 10cm x 55cm),, 4nos of hand towels(23.5cm x 38cm), 1no of adhesive medium drape sheet(size, 183cm x 183cm), 1no of adhesive large drape sheet(size 150cm x 250cm), 1no of, instrument table cover(150cm x 200cm), 1no of adhesive split sheet (size 228cm x, 260cm)., waterless chg and alcohol based handrub for hand hygiene, uniquely formulated, chlorhexidine gluconate ip 2.5% v/v (equivalent to 0.5% w/v chlorhexidine, gluconate) and ethanol ip 70% v/v with moisturizer and emollients to be used with, a twin purpose wall mount/bed-side dispenser. broad spectrum antimicrobial., waterless chg and alcohol based handrub for hand hygiene, uniquely formulated, chlorhexidine gluconate ip 2.5% v/v (equivalent to 0.5% w/v chlorhexidine, gluconate) and ethanol ip 70% v/v with moisturizer and emollients. broad, spectrum antimicrobial., high barrier disposable surgical drapes made of reinforced spunbond-film composite, which is a blue laminate of polypropylene nonwoven and a polyethylene film, offering absorbency yet imperviousness to fluid strike-through across the entire, drape material. it should be low-linting, non-breathable with an adhesive area,, wherever incorporated, containing hypoallergenic acrylate type adhesive covered, with a silicone coated paper liner and should also comply with the requirements of, iso 13485:2003 and iso 9001:2008. an extremity drape sheet with above features, should contain 1no of adhesive extremity drape sheet(size 228cm x 330cm)., high barrier disposable surgical drapes made of reinforced spunbond-film composite, which is a blue laminate of polypropylene nonwoven and a polyethylene film, offering absorbency yet imperviousness to fluid strike-through across the entire, drape material. it should be low-linting, non-breathable with an adhesive area,, wherever incorporated, containing hypoallergenic acrylate type adhesive covered, with a silicone coated paper liner and should also comply with the requirements of, iso 13485:2003 and iso 9001:2008. the pack with above features should contain, 1no of arthroscopy sheet with pouch (size 292cm x 304cm)., high barrier disposable surgical drapes made of reinforced spunbond-film composite, which is a blue laminate of polypropylene nonwoven and a polyethylene film, offering absorbency yet imperviousness to fluid strike-through across the entire, drape material. it should be low-linting, non-breathable with an adhesive area,, wherever incorporated, containing hypoallergenic acrylate type adhesive covered, with a silicone coated paper liner and should also comply with the requirements of, iso 13485:2003 and iso 9001:2008. the pack with above features should contain, 1no of stockinet (size 121cm x 30cm)., broad spectrum virucidal, bactericidal and fungicidal waterless alcohol based handrub, for hand hygiene, containing 75% v/v iso-propyl alcohol, moisturizer and, emollients with a wall-mounting/bed-side stand.100ml, high barrier disposable surgical drapes made of reinforced spunbond-film composite, which is a blue laminate of polypropylene nonwoven and a polyethylene film, offering absorbency yet imperviousness to fluid strike-through across the entire, drape material. it should be low-linting, non-breathable with an adhesive area,, wherever incorporated, containing hypoallergenic acrylate type adhesive covered, with a silicone coated paper liner and should also comply with the requirements of, iso 13485:2003 and iso 9001:2008. the pack with above features should contain, 2nos of adhesive drape sheet (size 91.5cm x 100cm)., incise drape which is antimicrobial, strong, conformable and breathable iodophor, impregnated polyester film coated with hypoallergenic adhesive for superior, adhesion. contain a clear plastic, fluid collection pouch around the incise drape., compatible with povidine iodine & chg preps.latex free,42 cm * 52 cm, product must be made of low-linting, nonwoven, absorbent fabric laminated to a, plastic film. must be resistant to fluid strikethrough. must be absorbent throughout, the entire drape, this eliminating the need to define a “critical zone”. must meet, flammability class 1 (cfr title 16 part 1610). components include: under arm, sheet (114cm x 100cm) - 1 no, operation tapes (10cm x 55cm) - 2 no, triangular, drape sheets - (91.5cm x 91.5cm x 129cm) - 2 nos, surgical drape that provides a vertical barrier to keep the c-arm isolated from the, sterile surgical field with a strong polyethylene film to withstand heavy manipulation, during use of the fluoroscope ensuring aseptic conditions during surgery. must be, one piece design with a clear plastic film allows for visualisation of the fluoroscope, during the operation. must have instrument pouches and tube organisers to keep, wires and tubes and instruments out of the operative side and a filter screen that, catches bone chips and tissue for specimen. must be latex-free for patient and, healthcare worker safety. dimensions - overall: 320cm x 213cm; incise area: 48cm, x 25cm; 5 units per case. must have iso certification, • self contained vials of spore strip b. stero-thermophilus population, • test tube containing modified soy tryptic broth as growth medium with, bromocresol purple dye, • easily identifiable color change to yellow in case of bacterial growth within 48, or before after incubating at 56 degree c temperature. should be compliant to iso, 11138-1:2006(en) part 1 and iso 11138-1:2006(en) part 3, • ansi/aami/ iso 11138-1:2006 & 11138-3: 2006, • should have a bsi kitemark certificate, • every box should contain quality assurance certificate with mention of spore, population & d- value, • self contained vials of spore strip b. atropheus population, • test tube containing modified soy tryptic broth as growth medium with, brothymol blue dye, • easily identifiable color change in case of bacterial growth within 48 hrs or before, after incubating at 37 degree c temperature., should be compliant to iso 11138-1:2006(en) part 1 and iso 11138-1:2006(en), part 2, • ansi/aami/ iso 11138-1:2006 & 11138-2: 2006, • should have a bsi kitemark certificate, • every box should contain quality assurance certificate with mention of spore, population & d- value, • rapid readout biological indicators containing a standardized, viable population, bacillus atropheus spores for eto sterilization cycles, • the indicator detects the presence of viable spores by the production of, fluorescence within 4 hours in conjunction with rapid readout incubator, • designed and certified as per iso 11138 and en 866.• should be compliant to iso, 11138-1:2006(en) part 1 and iso 11138-1:2006(en) part 2, • every box should contain quality assurance certificate with mention of spore, population, d- value & z value, • should have a bsi kitemark certificate, • should have fda clearance, • rapid readout biological indicators for steam sterilization containing a, standardized, viable population of bacillus stearothermophilus spores, • the indicator detects the presence of viable spores by the production of, fluorescence in 3 hours in conjunction with rapid readout incubator, • designed and certified as per iso 11138 and en 866., • should be compatible with the following cycles:, a) 121-123°c gravity steam sterilization cycle, b) 132-135°c vacuum-assisted steam sterilization cycles. should be compliant to, iso 11138-1:2006(en) part 1 and iso 11138-1:2006(en) part 3, • every box should contain quality assurance certificate with mention of spore, population, d- value & z value, • should have a bsi kitemark certificate, • should have fda clearance, • lead free, • heat sensitive chemical indicator self adherent tape, • should not leave any adhesive residue, for steam sterilization cycles., • color change should be from white to dark brown for easy identification after, processed in steam autoclaves of different time and temperature requirements,, within 15 minutes at 121 degree c and 3 minutes at 134 degree c.•class 1: confirms, to ansi/ aami/ iso 11140-1: 2005, • certificate of analysis should be available for every batch, • should have fda clearance, • test packs for monitoring vacuum formation in autoclave chambers., • test sheet along with penetration challenge material should be in a single easy, handled pack., • should be lead free., • weight per pack should be 110 to 125 gms.should be compliant to, ansi/aami/iso 11140-1:20051, • should be compliant to ansi/aami/iso 11140-5:20072, the 3m™ comply™ steam chemical indicator 1250 offers an off-white to black, color change when exposed to steam sterilization. can be used in all 121- 134˚c, (250-273˚f) gravity and vacuum assisted steam sterilization cycles. the strip is, perforated, allowing full or half-length use for different pack sizes. after processing,, the chemical indicator line will turn from off-white to black when exposed to steam, sterilization. strip is perforated enabling full or half-length usage depending on pack, size. 3m™ comply steam chemical indicator 1250 is designed to monitor all 121-, 134˚c (250-273˚ f) gravity and vacuum assisted steam sterilization cycles., • type 4 (category i4) internal indicators as categorized by iso 11140-1:2014, • two year shelf life, the 3m™ comply™ 1251 eo chemical indicator strip as an internal pack process, indicator to monitor all warm and cool cycles of 100% eo and eo/hcfc, (hydrochlorofluorocarbon) gas mixture sterilizer cycles. the chemical indicator bar, turns from red to green when exposed to critical parameters of the eo sterilization, process (i.e., gas concentration rh, time and temperature). designed to monitor all, warm and cool cycles of 100% eo and eo/hcfc (hydrochlorofluorocarbon) gas, mixture sterilizer cycles, strip is perforated enabling full or half-length usage depending on pack size, two year shelf life, • moving front chemical integrators, indicating accept or reject, to verify all, perimeters of steam sterilization together i.e. time, temperature and quality of, steam., • can be used for pack control monitoring of all 118-138ºc (245-280ºf) steam, sterilization cycles, should be compliant to bs/ en/ iso 11140-1: 2005, • should have 510 (k) registration, • should have a bsi kitemark certificate, • multiple enzymatic concentrate solution with lipases, cellulases, proteases and, amylases, • must act against all possible body secretions, compatible to all instruments, • fast acting within 2- 10 minutes, allow safe disposable via the drain after use, • leaves no residue after wash, stable formulation with near neutral ph., compliance to iso 13485, 1 l, • multiple enzymatic concentrate solution with lipases, cellulases, proteases and, amylases, • must act against all possible body secretions, compatible to all instruments, • fast acting within 2- 10 minutes, allow safe disposable via the drain after use, • leaves no residue after wash, stable formulation with near neutral ph., compliance to iso 13485, 100ml, label thickness 0.2 mm (± 0.01mm), label dimension 32x28mm, release layer material should be semi bleached kraft paper, visual appearance:, 1) corner cut piggy back label, 2) 2) white colored paper label, double liner labels:, release paper thickness liner 1 paper should be 0.05 mm (± 0.01mm) (1.97 mil), release paper thickness liner 2 paper should be 0.06 mm (± 0.01mm) (2.36 mil), label thickness 0.2 mm (± 0.01mm), label dimension 32x28mm, release layer material should be semi bleached kraft paper, visual appearance:, 1) corner cut piggy back label, 2) 2) white colored paper label, double liner labels:, release paper thickness liner 1 paper should be 0.05 mm (± 0.01mm) (1.97 mil), release paper thickness liner 2 paper should be 0.06 mm (± 0.01mm) (2.36 mil), • equipment should show remaining minutes left of bi incubation., • should be able to configure auto-reader remotely from a pc., • should have a built-in web app to allow create documentation that can be printed, or saved electronically., • shold have an option to connect to select sterile processing instrument tracking, systems., • auto reader, self calibrating, to read rapid attest bi, with ten incubation wells, • positive bi read-out time within 4 hrs by an audible alarm. should have iec, 61326‑1 electrical equipment for measurement, control and laboratory us+c11e, ‑emc requirements ‑ part 1: general requirements, • should comply with the emc requirements of the ce mark emc directive, 2004/108/ec., • equipment should show remaining minutes left of bi incubation., • should be able to configure auto-reader remotely from a pc., • should have a built-in web app to allow create documentation that can be printed, or saved electronically., • shold have an option to connect to select sterile processing instrument tracking, systems., • auto reader, self calibrating, to read rapid attest bi, with ten incubation wells, • positive bi read-out time of 1 hr to 3 hrs by an audible alarm. have iec 61326‑1, electrical equipment for measurement, control and laboratory use ‑emc, requirements ‑ part 1: general requirements, • should comply with the emc requirements of the ce mark emc directive, 2004/108/ec., • incubator should be compatible for both pre vacuum and gravity steam sterilizers, • should have a built-in web app to allow create documentation that can be printed, or saved electronically., • equipment should show remaining minutes left of bi incubation., • heating block temperature reading should be displayed, • positive bi read-out time within 1 hr by an audible alarm., • auto reader, self calibrating, to read rapid attest bi, with ten incubation wells, • compatible bi should be fda cleared, chemical indicator tape to monitor plasma sterilization by indicating a color, change of blue to pink for easy identification of processed and unprocessed loads/, packs., for use in sterrad® 100, 100s, nx® (standard and advanced cycles),, 100nx® (standard, flex, express and duo cycles), amsco® v-pro™ 1 (lumen, cycle), amsco® v-pro™ 1 plus (lumen and non lumen cycles), and amsco, v-pro™ max low temperature sterilization system (lumen, non lumen, and, flexible cycles) sterilizers., two year shelf life, process challenge device (pcd) that contains a 3-hour readout biological, indicator plus a steam chemical integrator for fast turnaround times for load, releases, class 5 integrator, moving front chemical integrators to verify all perimeters of steam sterilization, together i.e. time, temperature and quality of steam. read out indicates accept or, reject after processing., rapid bi, rapid readout biological indicators for steam sterilization containing a standardized,, viable population of bacillus stearothermophilus spores. the indicator detects the, presence of viable spores by the production of fluorescence in one to three hours., designed and certified as per iso 11138 and en 866., test packs for monitoring vacuum formation in autoclave chambers., test sheet along with penetration challenge material should be in a single easy, handled pack., should be lead free, weight per pack should be 110 to 125 gms, early warning sheet indicates impending sterilizer failure earlier than the bowie, dick test sheet, • rapid readout biological indicators for steam sterilization containing a, standardized, viable population of bacillus stearothermophilus spores, • the indicator detects the presence of viable spores within 1 hour in conjunction, with super rapid readout incubator, • designed and certified as per iso 11138 and en 866., • should be compatible with the pre vacuum cycle of 132°c to 135°c, should be, compliant to iso 11138-1:2006(en) part 1 and iso 11138-1:2006(en) part 2, • every box should contain quality assurance certificate with mention of spore, population, d- value & z value, • should have a bsi kitemark certificate, • should have fda clearance, • moving front chemical integrators, indicating accept or reject, to verify all, perimeters of steam sterilization together i.e. time, temperature and quality of, steam., • can be used for pack control monitoring of all 118-138ºc (245-280ºf) steam, sterilization cycles, should be compliant to bs/ en/ iso 11140-1: 2005, • should have 510 (k) registration, • should have a bsi kitemark certificate pack of 500/box,2 box /case, the equipment must be a forced air warmer to deliver effective forced – air patient, warming, it should be microprocessor based handy and with accurate temperature, sensor system. flicker-free operation defined as meets iec 61000-3-3 standard, it, should have audible and visual alarms in case of over temperature, it should have, washable protective hose cover, the equipment should be pole and bed mountable,, each equipment should be supplied with stand.unit weight: 7kg,, airflow setting:2 speed, -adjustable up to 44 cfm (20.8 l/s), the equipment must be a forced air warmer to deliver effective forced – air patient, warming, it should be microprocessor based handy and with accurate temperature, sensor system. flicker-free operation defined as meets iec 61000-3-3 standard, it, should have audible and visual alarms in case of over temperature, it should have, washable protective hose cover, the equipment should be pole and bed mountable,, each equipment should be supplied with stand.unit weight: 4.5 kg,, airflow setting:one speed, non-adjustable up to 44 cfm (20.8 l/s), full body blanket,material that is soft, conformable, lightweight, and, radiolucent,uniform perforation pattern across the blanket surface ensures even, convective warming,non-inflated foot drapes guard against thermal injury to the, heat-sensitive feet and lower legs,patented blanket designs that provide even heat, distribution size 84 x 36 in (213 x 91 cm), pediatic full body blankes designed to bend in order to accommodate a wide range, of surgical procedures and positions,soft, conformable, lightweight, and, radiolucent,non-inflated foot drapes guard against thermal injury to the heatsensitive, feet and lower legs and patented blanket designs that provide even heat, distribution size 60 x 36 in (152 x 91 cm), it is designed to bend in order to accommodate a wide range of surgical procedures, and positions,material that is soft, conformable, lightweight, and radiolucent and, continuous adhesive strip to secures blanket to patient size 60 x 36 in (152 x 91 cm), pediatric long blanket,tube shape blanket which surrounds patient with warm air,, is designed to bend in order to accommodate a wide range of surgical procedures, and positions.size 74 x 8.5 in (188 x 21 cm), it is designed to bend in order to accommodate a wide range of surgical procedures, and positions,material that is soft, conformable, lightweight, and radiolucent,passthrough, slit design allows for flexible patient positioning and accommodates the use, of a drawsheet,patented fluid outlets minimize pooling of fluids on the surface of the, blanket size 74 x 36 in (188 x 91 cm), it is designed to bend in order to accommodate a wide range of surgical procedures, and positions.two reselable hose ports and patented fluid outlets minimize pooling, of fluids on the surface of the blanket size 60 x 32 in (152 x 81 cm), it is designed to bend in order to accommodate a wide range of surgical procedures, and positions,should have integrated adhesive ,foot drape,and have large surgical, access window size 84 x 36 in (213 x 91 cm), lithotomy underbody blanket,material that is soft, conformable, lightweight, and, radiolucent,advanced blanket designs warm the patient while providing, full,patented fluid outlets minimize pooling of fluids on the surface of the blanket, unrestricted patient access64 x 36 in (160 x 91 cm), full access underbody blanket ,material that is soft, conformable, lightweight, and, radiolucent,advanced blanket designs warm the patient while providing, full,patented fluid outlets minimize pooling of fluids on the surface of the blanket, unrestricted patient access,size 84 x 36 in (221 x 91 cm), sterile full access underbody blanket,material that is soft, conformable,, lightweight, and radiolucent,advanced blanket designs warm the patient while, providing full,patented fluid outlets minimize pooling of fluids on the surface of the, blanket unrestricted patient access, size 84 x 36 in (221 x 91 cm), multi position upperbody blanket 622,material that is soft, conformable,, lightweight, and radiolucent,it is designed to bend in order to accommodate a wide, range of surgical procedures and positions,provides coverage for additional, positions and accommodates a wider range of surgical procedures- supine, prone,, and lateral, beach chair, steep trendelenburg (robotics), lithotomy, and plastic, surgery position,size 78 x 24 in (198 x 61 cm), a non-invasive deep tissue body temperature monitoring sensor with a memory chip, that facilitates a two hour continuous visual representation of the patient temperature, trend on a control unit. the sensor should have a medical grade adhesive that is, biocompatible with the human skin. dimensions: 1.6inch diameter and 0.2 inches, thickness. 25 units per case. must be fda cfg, iso 13485, iec and ce certified, a non-invasive, temperature monitoring unit that can be used to continuously, montior and record core temperature. the machine should have a memory display of, at least 90 minutes. weight of the control unit should be less than 150g and the, length of the sensor cable should be over 350cm., silver impregnated foam dressing size/packing, silver impregnated foam dressing size/packing:, latex free polyester cast bandage is water activated, latex free polyester cast bandage is water activated, cotton and viscose pad, binds bacteria, microbes,pus and debris. with dacc, cotton and viscose pad, binds bacteria, microbes,pus and debris. with dacc, nano crystalline silver dressing made up of rayon polyester, nano crystalline silver dressing made up of rayon polyester, sterile transparent dressings for iv lines, sterile transparent dressings for iv lines, chlorohexidine gauze dressing, electrochemically processed aqueous gel based solution with patented technology, tolerance irrigation solution strictly us-fda approved .packaging = 60ml, bottle gel, electrochemically processed aqueous gel based solution with patented technology, maximise tolerance irrigation solution strictly us-fda approved .packaging = 100, ml bottle gel, electrochemically processed aqueous gel based solutionwith patented technology, maximise tolerance irrigation solution strictly us-fda approved .packaging =120, ml bottle gel, electrochemically processed aqueous gel based solution with patented technology, maximise tolerance irrigation solution strictly us-fda approved .packaging = 200, ml jar, electrochemically processed aqueous gel based solution with patented technology, maximise tolerance irrigation solution strictly us-fda approved .packaging = 400, ml jar, electrochemically processed aqueous based solution with microcyn technology, patented: maximise tolerance irrigation solution.strictly us-fda approved, packaging:- = 100ml bottle, electrochemically processed aqueous based solution with patented technology, maximise tolerance irrigation solution.strictly us-fda approved packaging = 500, ml, electrochemically processed aqueous based solution with patented technology, maximise tolerance irrigation solution. strictly us-fda approved packaging:- =, 1000 ml bottle (1 litre), electrochemically processed aqueous based solution with with patented technology, for disinfectant maximise tolerance irrigation solution. strictly us-fda approved, packaging:- = 1000 ml bottle (1 litre), electrochemically processed aqueous based solution with patented technology, ecosafe disinfectant maximise tolerance irrigation solution. strictly us-fda, approved. packaging :- = 5 litre jerricane, anti microbial silver dressing with flexible polyester mesh open weave structure, anti microbial silver dressing with flexible polyester mesh open weave structure, anti microbial silver dressing with flexible polyester mesh open weave structure, iodine impregnated theatre incise drape, antimicrobial silver dressing with nanocrystalline technology, suction microhatches, suction micro hook, suction micro hook, preyer suction finder, suction round cut knife, suction round cut knife, suction round cut knife, suction knife, suction knife, suction dissector, suction dissector, suction dissector for attik, suction dissector for attik, suction dissector for sinus tympani, suction dissector for sinus tympani, suction curette, suction curette, suction dissector, suction dissector, system screen basket for panetti instruments, suction adapter, haemostatic dressing in sponge/pad form made of 100% natural biopolymer with, a net positive charge, gamma sterilized & moisture proof packing. manufactured, in india, gmp & iso 13485. certified by european ce mark / usfda size:5x5, cm, haemostatic dressing in sponge/pad form made of 100% natural biopolymer with, net positive charge, gamma sterilized & moisture proof packing. manufactured, in india, gmp & iso 13485. certified by european ce mark / usfda size: 8x5, cm, disposable blade for mcgrath video alryngoscope, battery for mcgrath video laryngoscope, reusable nellcor covidien spo2 sensor adult (ds100a) for nellcor pulse oximeter, reusable nellcor covidien spo2 sensor neonatal (dy-s) for nellcor pulse, oximeter, reusable nellcor covidien spo2 sensor pediatric (flexmax-p) for nellcor, pulse oximeter, disposable nellcor covidien spo2 sensor for neonatal for nellcor pulse oximeter, bis sensor -quotro, elastic shoulder immobiliser (us fda certified – registration no 3005037196):-, should have a scientific design providing 6 way immobilisation, proper ventilation,, comfort and be able to be used in patients confined to bed or with open shoulder, wounds. should have additional shoulder cups for improv immobilisation, grip on, injured shoulder & enhance patient confidence. (xxl), clavicle brace velcro (us fda certified – registration no 3005037196):-reverse, buckle fastening with hook loop tapes to offer better tightening & grip and pu foam, padding to ensure no underarm rashes. figure of 8 design with lateral vctor for, ensuring linear union of the bone, easy application & tightening of the braace. (ch), clavicle brace velcro (us fda certified – registration no 3005037196):-reverse, buckle fastening with hook loop tapes to offer better tightening & grip and pu foam, padding to ensure no underarm rashes. figure of 8 design with lateral vctor for, ensuring linear union of the bone, easy application & tightening of the braace., colour fastness. (large), knee cap comfeel (us fda certified – registration no 3005037196):- should be, anatomically shaped with 3d knitting and reduced compression spot to ensure no, patellar pressure. should have a bi layered construction containing dermophillic, cotton inside for comfort in all weather conditions & nylon outside for durability &, colour fastness., r.o.m.knee brace(us fda certified – registration no 3005037196):- should be, constructed from strong aluminium frames & neoprene fabric. should have a rom, hinge on either side which is a sophisticated multi point graduate d, mechanism (mpgm) that can be adjusted to fix any angle of flexion or provide, controlled motion between any two angles by a simple pull – rotate – push, dial locking mechanism. (universal (18”) special (22”)), cool pack knee wrap (us fda certified – registration no 3005037196):-, dessigned to provide cold compress to deliver the benefits of cryotherapy w, ith compression after soft tissue trauma. the gel pouch should be made of soft, & flexible poly vinyl film filled with high performance hydrophilic gel. fabric on, the inner side to prevent cryo burns and ensure easy application. the snap button, on the fabric pouch allows easy insertion & removlal of gel pack.the anatomical, knee wrap design should ensure best coverage of the affected knee and the three, elasticized straps should ensure good compression of the gel against the knee for, fast therapy and recovery. (universal), elbow support (us fda certified – registration no 3005037196):- should be, made of high quality nylon – spandex yarn to ensure 4 way stretchability, snug fitting & excellent splint compression. should be anatomically shaped, with extra stretch at elbow to allow easy elbow movement, better comfort, better, compression & grip. should have an elasticized band to provide controlled &, targeted compression at the site of inflammation. (medium), elbow support (us fda certified – registration no 3005037196):- should be, made of high quality nylon – spandex yarn to ensure 4 way stretchability, snug fitting & excellent splint compression. should be anatomically shaped, with extra stretch at elbow to allow easy elbow movement, better comfort, better, compression & grip. should have an elasticized band to provide controlled &, targeted compression at the site of inflammation. (large), elbow support (us fda certified – registration no 3005037196):- should be, made of high quality nylon – spandex yarn to ensure 4 way stretchability, snug fitting & excellent splint compression. should be anatomically shaped, with extra stretch at elbow to allow easy elbow movement, better comfort, better, compression & grip. should have an elasticized band to provide controlled &, targeted compression at the site of inflammation. (xl), wrist splint ambidextrous ( us fda certified – registration no 3005037196):-, should be made of high quality, strong & durable elasstic webbing. should have, removable aluminium splint to allow customized dorsi flexion , enhanced grip, immobilization. design should allow for thumb abduction to ensure, reduced fatigue & pain and improved healing. (small), wrist splint ambidextrous ( us fda certified – registration no 3005037196):-, should be made of high quality, strong & durable elasstic webbing. should have, removable aluminium splint to allow customized dorsi flexion , enhanced grip, immobilization. design should allow for thumb abduction to ensure, reduced fatigue & pain and improved healing. (medium), leg traction brace (us fda certified – registration no 3005037196):- should, have pu sandwiched fabric for cushioning & strong grip. skin facing layer to ensure, good frictional property and multiple hook loop tapes to ensure controlled, compression & easy application w/o loosening. should have a large skin contact, area to eliminate need of adhesives or over tightening. should have inbuilt, spreader bar & traction bar. (large), leg traction brace (us fda certified – registration no 3005037196):- should, have pu sandwiched fabric for cushioning & strong grip. skin facing layer to ensure, good frictional property and multiple hook loop tapes to ensure controlled, compression & easy application w/o loosening. should have a large skin contact, area to eliminate need of adhesives or over tightening. should have inbuilt, spreader bar & traction bar. (xl), heating pad ortho (us fda certified – registration no 3005037196):- should, have ptfe extruded heating element to ensure complete protection against electric, shock, high temperature stability & long functional life. should be made of soft, fleece fabric & ensure no hot spots. should have water repellant, thermostat, 90 minute shutoff with led indicator and 40* - 80* temperature range., (standard & special), cool pack (us fda certified – regisration no 3005037196):- the gel pouch, should be made of soft & flexible pu/pvc for effective cooling containing high, performance hydrophilic gel. should have a fabric cover with straps for convenient, use and to prevent cryo burns. ( (small & universal), coccyx cushion seat(us fda certified – registration no 3005037196):- should, be made from high density memory foam with high viscoelastic properties,, excellent cushioning & long functional life. should have an anatomical hole &, recess design to minimize the pressure on the anal area & tail bone and distribute, the body weight equally. should have non slip rubber fabric & a highly, stretchable top to conform to body contours. (universal), ortho stockinete 10 mtrs(us fda certified – registration no 3005037196):-, should be made from high quality stapled cotton with seamless fabric knitted, on a state of art looms to provide durable, comfortable & hypoallergenic interface, between skin and various orthotic or prosthetic devices. (50mm) etc
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