WBHF/CMS/HST/1QC-36-2018 /NABL/2018-20/061/ GROUP-V

Esbachs Reagent

Estradiol Elisa Kit

Ethanol 95% v/v (Rectified Spirit) - 100 ml

Ethanol 95% v/v(Rectified Spirit)

Ether Solvent

FERRITIN- Elisa

Fixer (X-Ray film)

Formaldehyde Tablet

Formalin Solution 40%

fPSA - Elisa

French Chalk

FSH - Elisa

FT3- Elisa

FT4- Elisa

Furazolidone Antibiotic Disc

Gamma Benzene Hexachloride 1% w/v + Cetrimide 0.1% w/v

Gentamicin Antibiotic Disc

Giemsa Stain 25 mg.

Glacial Acetic Acid

Glucose Test Kit

Glucose-6-Phosphate Dehydrogenase- Test Kit

Glucostix

Gluteraldehyde Solution 2% for Instrument Sterilisation

Glycerin I.P.

Glycin Irrigation Fluid

Gram Stain Kit

H2S Strip Kit

Haemodialysis Fluid with Bi-Carb

Hamatoxyllin Eosin Stain Powder

Hand Disinfactant : Each 100 gm Soln. contains : 2- Propanol- 45g, 1-Propanol- 30g, Ethyl-Hexadecyl- Dimethyl - Ammonium Ethyl Sulphate - 0.2 g

Hand Rub Soln.: 0.5% W/V Chlorhexidine Gluconate & 70 % v/v Ethanol

HbA1C Test kit

HbsAg (Elisa) Kit Specification: 1. Microplate ELISA coated with monoclonal antibodies to HBsAG. 2. The assay should be able to detect surface antigen to Hepatitis B virus. 3. Adequate documents detailing the principle, components, bio-safety, methodologies, validity criteria, interpretation of results, performance characteristics, storage conditions limitation of assays, manufacturing & expiry dates should be provided with each kit. 4. The kit to be procured should have approval of the statutory authority in its country of origin. 5. In case of imported kits it should have been registered and licensed in India by DCG(I) . 6. In case of indigenous manufacturers they shall have license issued by the competent authority defined under Drugs and Cosmetics Act, 1940, after appropriate evaluation by the centers approved by DCG(I). 7. The kit should have minimum shelf life of 60% or 12 months (whichever is more) at the port of discharge of consignees. 8. The assay component should include reactive and non-reactive controls. 9. The assay should have sensitivity of more than or equal to 99% and specificity of more than or equal to 98% 10. The assay should have analytical sensitivity of detecting less than or equal to 0.5ng/ml. 11. The manufacturer/authorized agent should ensure maintenance of cold chain during storage & transport the kits at 20 C - 80 C . The cumulative time temperature indicator technology used should be pre-qualified by WHO. 12. The Kit size should be 96 tests /kit. 13. The item should be Up graded from III Generation to IV Generation Test Kit in the light of BTS TRG recommendation dated 12th January 2015.

HBsAg (Rapid) Kit Specification: 1. Should be solid phase/particle coated with monoclonal antibodies to HBsAg. 2. The assay should be able to detect surface antigen to Hepatitis B virus. 3. Adequate documents detailing the principle, components, bio-safety, methodologies, validity criteria, interpretation of results, performance characteristics, storage conditions, limitation of assays, manufacturing & expiry dates should be provided with each kit. 4. The kit to be procured should have approval of the statutory authority in its country of origin. 5. In case of imported kits it should be registered and licensed in India by DCG(I) . 6. In case of indigenous manufacturers they should be licensed by the competent authority defined under Drugs and Cosmetics Act, 1940, after appropriate evaluation by the centers approved by DCG(I). 7. The kit should have minimum shelf –life of 60% or 12 months (whichever is more) at the port of discharge of consignees. 8. The total procedure time shall not be more than 30 minutes. 9. The assay component should include positive and Negative control in each pack of 50 tests. 10. The assay should have sensitivity of more than or equal to 99% and specificity of more than or equal to 98%. 11. The assay should have analytical sensitivity of detecting less than or equal to 0.5ng/ml. 12. The manufacturer/authorized agent should ensure maintenance of cold chain during storage & transport the kits at 20 C - 80 C . The cumulative time temperature indicator technology used should be pre-qualified by WHO. 13. The pack size should not be more than 50 tests wherein each test in individually packed. 14. The item should be Up graded from III Generation to IV Generation Test Kit in the light of BTS TRG recommendation dated 12th January 2015.

HCV (Elisa) Kit Specification: 1. Microplate ELISA Coated with recombinant / synthetic peptide antigens for core, NS3, NS4 and NS5. 2. Adequated documents detailing the principle, components, bio-safety, methodologies, validity criteria, interpretation of results, performance characteristics, storage conditions, limitation of assays ,manufacturing & expiry dates should be provided with each kit. 3. The kit to be procured should have approval of the statutory authority in its country of origin. 4. In case of imported kits it should have been registered and licensed in India by DCG(I). 5. In case of indigenous manufactures they shall have license issued by the competent authority defined under Drugs and Cosmetics Act, 1940, after appropriate evaluation by the centers approved by DCG(I). 6. The kits should have minimum shelf-life of 60% or 12 months (whichever is more) at the port of discharge of consignees. 7. The assay component should include reactive and non-reactive controls. 8. The assay should have a sensitivity more than or equal to 99% and specificity of more than or equal to 98%. 9. The manufacturer / authorized agent should ensure maintenance of cold chain during storage & transport the kits at 20 C - 80 C. The cumulative time temperature indicator technology used should be pre-qualified by WHO. 10. The kit size should be 96 test/.kit. 11. The item should be Up graded from III Generation to IV Generation Test Kit in the light of BTS TRG recommendation dated 12th January 2015.

HCV (Rapid) Kit Specification: 1. Should be solid phase/particle coated with recombinant and / or synthetic peptide antigens for Core,NS3,NS4 and NS5. 2. Adequate documents detailing the principle, components, bio-safety, methodologies, validity criteria, interpretation of results, performance characteristics, storage conditions, limitation of assays, manufacturing & expiry dates should be provide with each kit. 3. The kit to be procured should have approval of the statutory authority in its country of origin 4. In case of imported kits it should have been registered and licensed in India by DCG(I). 5. In case of indigenous manufactures they should be licensed by the competent authority defined under Drugs and Cosmetics Act, 1940, after appropriate evaluation by the centers approved by DCG(I). 6. The kit should have minimum shelf-life of 60% or 12 months (whichever is more) at the port of discharge of consignees. 7. The total procedure time shall not be more than 30 minutes. 8. The assay component should include positive and Negative control in each pack of 50 tests. 9. The assay should have sensitivity of more than or equal to 99% and specificity or more than or equal to 98%. 10. The manufacture / authorized agent should ensure maintenance of cold chain during storage & transport the kits at 20 C - 80 C. The cumulative time temperature indicator technology used should be pre-qualified by WHO. 11. The Pack size should not be more than 50 tests wherein each test is individually packed. 12.The item should be Up graded from III Generation to IV Generation Test Kit in the light of BTS TRG recommendations dated 12th January 2015.

HDL Cholesterol - D (Immunoterbedimetric) Test Kit

Hepatitis A test Kit

Hepatitis E test Kit

HIV (Elisa) Kit Specification: 1. Should be solid phase microplate Coated HIV I & II Recombinant and/or synthetic peptide antigens. 2. The assay should detected HIV 1 and II antibodies. 3. Adequate documents detailing the principal, components, details of antigen for antibody detection of HIV 1and 2, bio-safety, methodologies, validity criteria, interpretation of results, performance characteristics, storage condition, limitation of assays, manufacturing & expiry dates should be provide with each kit. 4.The kit should have approval of the statutory authority in its country of origin. 5.In case of Imported kits it should be registered and licensed in India by DCG(I) 6. In case of indigenous manufacturers should be licensed issued by the competent authority defined under Drugs and Cosmetics Act, 1940 & also be evaluated by the centers approved by DCG(I) 7.The kit should have minimum shelf-life of 60% or 12 months (whichever is more) at the port of discharge of consignees . 8.The assay component should includ reactive and non-reactive controls with each kit. 9.The assay should have sensitivity level of more than or equal to 99.5% and specificity level of more than or equal to 98%. 10.The manufacture / authorized agent should ensure maintenance of cold chain during storage and transport the kits at 20 C - 80 C . The cumulative time temperature indicator technology used should be pre-qualified by WHO. 11. The pack size should be 96 tests/kit. 12.The item should be Up graded from III Generation to IV Generation Test Kit in the light of BTS TRG recommendation dated 12th January 2015.

HIV (Rapid) Testing Kits [By Principal of Enzyme Immuno Assay, Agglutination, or any other Principle] Specification :- 1. Should be a solid phase coated HIV I & HIV II recombinant and / or synthetic peptide antigens. 2. The assay should detect HIV I & II antibodies in plasma,serum or whole blood. 3. Adequte documents detailing the principle , components, details of antigen for antibody detection of HIV I & II, bio-safety, methodologies, validity criteria, interpretation of results, performance characteristics, storage conditions, limitation of assays, manufacturing & expiry dates should be provided with each kit. 4. The kit should have approval of the statutory authority from the country of origin. 5. In case of imported kits it should be registered and licensed by DCG(I). 6. In case of indigenous manufacturers should be licensed by the competent authority defined under Drugs and Cosmetics Act 1940,also be evaluated by the centers approved by DCG(I). 7. The kit should have minimum shelf-life of 60% or 12 months (whichever is more) at the port of discharge of consignees. 8. The time required for performing the test should not be more than 30 minutes. 9. The control dot/band should be able to detect the presence of human immunoglobulins and should not be just a “procedural control” or meant for merely checking the flow of reagents or integrity of the antigen. 10. The assay should have sensitivity of more than or equal to 99.5% and specificity of more than or equal to 98%. 11. The manufacturers should ensure that : a. The test kit should be packed such that there is a provision to conduct single test at a time; b. The assay components should include HIV positive and negative serum control sufficient for conducting 20% of the tests (10% negative and 10% positive controls);and c. The pack size of HIV rapid test kits should not be more that 50 tests per kit. 12. The manufacturer/authorized agent should ensure maintenance of cold chain during storage & transport the kits at 20 C - 80 C. The cumulative time temperature indicator technology used should be pre-qualified by WHO. 13. The item should be Up graded from III Generation to IV Generation Test Kit in the light of BTS TRG recommendation dated 12th January 2015.

HsCRP Test Kit

Hydrogen Peroxide 11% w/v +diluted Silver Nitrate 0.01% w/v

Hydrogen Peroxide Soln. (20Vol) I.P.

Imipenem/Cilastatin Antibiotic Disc

Immersion Oil

Indole strip

Iodine Crystal , A.R.

Isoprophyl Alcohol IP 70% v/v

Kanamycin Antibiotic Disc

KIT FOR EARLY DIAGNOSIS OF PREGNANCY BY IMMUNOLOGICAL METHOD (HCG)

KOH Solution 10% L

Lactate Test Kit

LDL Direct Diagnostic Kit

Leishman Stain Soln.

Levofloxacin Antibiotic Disc

LH kit - Elisa

Lincomycin Antibiotic Disc

Lineazolid Antibiotic Disc

Lipase Test Kit

Liquid Paraffin I.P. (Heavy)

Liquified Phenol I.P. (Carbolic Acid)

Lomefloxacin Antibiotic Disc

Mac Conkey Agar

Magnesium Sulphate I.P.

Malachite Green

MB/BACT Antibiotic Suppliment Kit

Meropenem Antibiotic Disc

Methyl Alcohol

Methyl Violet

METHYLENE BLUE Liquid

METHYLENE BLUE Powder

Micro Protein Test Kit

Minocyclin Antibiotic Disc

Moxifloxacin Antibiotic Disc

Mueller Hintone Agar

Multistrips- 8 Parameter (Alb,Glucose, pH, Ketone, Blood, Bilirubin, Urobilinogen & Nitrite)

Muritic Acid

Nalidixic Antibiotic Disc

Netilmycin Antibiotic Disc

Nitric Acid

Nitrofurantoin Antibiotic Disc

Norfloxacin Antibiotic Disc

O.T.sterilization solution for fumigation/mopping, in powder form, Composition :-Potassium Mono per Sulphate (Triple Salt )- 40% to 50 %, Sodium C 10-13 Alkyl benzene Sulphate - 10% to 20% and Sodium Chloride - 1% to 5%.

Ofloxacin Antibiotic Disc

Paraffin Wax 58 c to 60 c

Paraffin Wax 60 c X 62 c

Penicillin Antibiotic Disc

Peptone

pH paper range 1 to 14

Piperacillin Antibiotic Disc

Pipercillin-Tazobactam Antibiotic Disc

Poly Sodium Citrate

Potassium Iodide

Potassium Permanganate I.P.

PPA Media

Primary Antibody ER

Primary Antibody HER

Primary Antibody PR

Progesterone Elisa Kit

PROLACTIN - Elisa

Providone Iodine cleansing solution 7.5% w/v surgical scrub

PT Reagent

Purified Water I.P.

PYR Reagent

PYR strip

Rapid diagnostic kit for Kala-azar (RK-39)

Rheumatoid Factor (Immunoterbedimetric) Test Kit

Rifampicin Antibiotic Disc

Roxithromycin Antibiotic Disc

RPR (Rapid Plasma Reagin) Kit Specification: 1. The indigenous RPR (Rapid Plasma Reagin) kits should have been manufactured under manufacturing license issued by the State Licensing Authority under the Drugs and Cosmetics Act. The imported kits should have been imported under import License issued by the DCG(I) under Drugs and Cosmetics Act. 2. The assay should allow for qualitative and semi quantitative determination of Reagin antibodies in serum or plasma for sero-diagnosis of syphilis based on flocculation principle using non treponemal antigens. 3. The assay should be suitable to perform with either serum or plasma 4. The assay should have sensitivity of 85% or more in primary syphilis and a specificity of 93% or more. 5. The assay should be calibrated to WHO reference serum and the same should be supported by statements in kit insert and certificate from manufacturer. 6. The test should be able to yield results within 20 minutes. 7. The pack size of RPR test kit should be less than or equal to 50 tests per kit. 8. The assay components should include positive and negative serum control sufficient for conducting 20% of the tests (10% negative and 10% positive controls). 9. The kit should have all essential accessories required for the test such as cards, droppers, applicator etc. in adequate quantities for the number of tests to be performed. 10. The kit should have minimum shelf-life of 60% or 12 months (whichever is more) at the port of discharge of consignees. 11. The cumulative time temperature indicator technology used should be pre-qualified by WHO. 12. Literature, detailing the components, methodologies, validity criteria, performance characteristics, storage conditions, manufacturing and expiry dates should be provided with each kit. 13. The item should be Up graded from III Generation to IV Generation Test Kit in the light of BTS TRG recommendation dated 12th January 2015.

Sabouraud Dextrose Agar (SDA) with CC

Serum Billirubin Test kit

SGOT Test Kit

SGPT Test Kit

Simmons Citrate Agar

Sodium Hypochloride – 500 ml Bot.

Solution for instrumental sterilization in powder form, Composition : Sodium Perborate Monohydrate 50% w/w (0.26% per acetic acid)

Sparfloxacin Antibiotic Disc

Streptomycin Antibiotic Disc

Surface Disinfactant Soln (Each 100 gm Contains: 1,6 Di-Hydroxy 2,5 Di-Oxyhexane (Chemically Bound Formaldehyde ) - 11.2 gms , Glutaraldehide 5 gm , Benzalkonium Chloride 5 gm, Alkyl Urea Derivatives 3 gms

T4 - Elisa

TCBS Agar

Teicoplanin Antibiotic Disc

Tetracyclin Antibiotic Disc

Ticarcillin/Clavulanic Acid Antibiotic Disc

Tobramycin Antibiotic Disc

Toludine Blue

Total Protein Test Kit

Total PSA Elisa Kit

TREPONEMAL-SPECIFIC RAPID (POINT-OF-CARE) DIAGNOSTIC TEST FOR SYPHILIS (POC Test Kit) TECHNICAL SPECIFICATION : o The assay should have solid phase coated with synthetic or recombinant type of Treponema Pallidum antigens. o The assay may be based on any of the rapid test principles: o (Immunoconcentration/Dot blot Immunoassay (vertical flow), dip stick and comb assay. o The assay should quantitatively detect total anti-treponemal antibody (IgG and IgM) in whole blood, serum or plasma for serological diagnosis of syphilis in all stages of infection. o The assay should have an in-built positive and negative control for testing the validity of the test kits. o The assay should have reactive and non-reactive controls with each kit in adequate volume (minimum 10% of pack size). o The kit should have 5/6th of the shelf life or 12 months before expiry (whichever is more) at the item of receipt by the consignee. o Adequate literature detailing the principle, components, methodologies, validity criteria, bio-safety , performance characteristics, storage conditions, limitation of assay, manufacture and expiry dates and methods of disposal should be provided with each kit. o The imported rapid kit should have approval of the statutory authority in its country of origin. The imported kits should have been registered and licensed in India by the Central Drugs Standard Control Organisation (CDSCO). o In case of indigenous manufacturers they should have a valid licence issued by the competent authority defined under Drugs and Cosmetics Act, 1940, after appropriate evaluation by the centres approved by the CDSCO. o The assay should have sensitivity of 90% or more and specificity of 95% or more and the same should be supported by statements in kit insert and certificate from National Institute of Biological Sciences. o The assay should be calibrated by WHO reference serum and the same should be supported by statements in kit insert and certificate from the manufacturer. o The manufacturer should ensure the following: >> The test should be packed such that there is a provision to conduct single test at a time. >> The pack size of test kits should be in 50 (for peripheral health levels) and 100 tests per kit (for secondary and tertiary health care level) but not more than 100 tests per kit. o The manufacturer /authorized agent should ensure maintenance of cold chain during storage and transport of kits at 20 C to 80 C. o Total procedure time should not be more than 30 minutes. o The test kit should be supplied with micro-pipette of 1 micro litre volume o The test kit should be supplied with sterilized disposable lancet one for each test o Alcohol soaked swab should be supplied with one for each test.

Tri Sodium Citrate

Triglyceride Test Kit

Trimethoprim Antibiotic Disc

TSH - Elisa

TSI Agar

Typhoid IgM Test Kit

Urea - ( GLDH) Reagent Kit

Urea -(Berthelot) Reagent Kit

Urea Agar Base

Urea Solution Sterile 40%

Uric Acid Test Kit

Uristix (10 Parameters)

Vancomycin Antibiotic Disc

VDRL Kit - latex kit

Vitamin D Elisa Kit

White Soft Paraffin I.P.

Whole Blood Finger-Prick HIV Test kit. Technical Specifications 1. The indigenous HIV antibody rapid test kits should have a valid license issued by the competent authority defined under Drugs & Cosmetics Act. 1940 after appropriate evaluation by the centres approved by DCG(I). The imported rapid test kits should have the approval of the statutory authority in the country of Origin/manufacture and should satisfy the requirements of Drugs and cosmetics act in India. The imported kits should also get evaluated in our country 2. The assay should be able to detect antibodies of HIV-I and HIV-2 and all the subtypes by detection of antibodies by the agglutination, Enzyme Immune Assay or any other principal. 3. The assay should have sensitivity of 99.5% or more and specificity of 98% or more as per data from an identified national reference laboratory. 4. The assay should have solid phase/particles coated with synthetic and/or recombination or both types of antigens of HIV1 & HIV2. 5. Total procedure time should not be more than 30 minutes. 6. The manufactures should ensure that a. The test kit should be packed such that there is a provision to conduct single test at a time. b. The assay components should include HIV positive and negative serum controls sufficient for conducting 20% of the tests (10% negative & 10% positive controls); and c. The pack size of HIV rapid test kits should not be more than 50 tests per kit.

Widal Antigen Test Kit

XLD Agar

Xylene

ABSORBABLE GELATINE SPONGE IP 66

Access guidewire - Nitinol core wire. Straight Tip with hydrophilic coating. Working Length : 450 cm, Outer Dia : 0.035"

Adhesive (Copolymer) based Silk Tape, non-elastic tape with strong tensile strength, 1.25 cm (minimum.) x 9 m (minimum) .

Adhesive (Copolymer) based Silk Tape, non-elastic tape with strong tensile strength, 2.50 cm (Minimum) x 9m (minimum) .

Adhesive (Copolymer) based Silk Tape, non-elastic tape with strong tensile strength, 5.00 cm (Minimum) x 9m (minimum) .

Adhesive (Copolymer) based Silk Tape, non-elastic tape with strong tensile strength, 7.50 cm (Minimum) x 9m (minimum) .

Adhesive Elastic Bandage (10cm X 4 mtr.)

Adhesive Elastic Bandage (10cm X 6 mtr.)

ADHESIVE PLASTER PLAIN 10 CM x 10 M

ADHESIVE PLASTER PLAIN 5 CM x 10 M

ADHESIVE PLASTER PLAIN 7.5 CM x 10 M

Adhesive, Paper Adhesive Plaster 2.50 cm (Minimum) x 9m (minimum), Breathable and comfortable, Non woven adhesive Tape

Adhesive, Paper Adhesive Plaster 1.25 cm (minimum.) x 9 m (minimum) ,Breathable and comfortable, Non woven adhesive Tape

Adhesive, Paper Adhesive Plaster 5.00 cm (Minimum) x 9m (minimum) , Breathable and comfortable, Non woven adhesive Tape

Adhesive, Paper Adhesive Plaster 7.50 cm (Minimum) x 9m (minimum) , Breathable and comfortable, Non woven adhesive Tape

Adhesive, sterilized umbilical cotton tape width 3 mm , length 75 cm

Adhesive, Transparent film Dressing with window frame delivery style, Waterproof, sterile, Bacterial and viral barrier, high adhesive but skin friendly with easy stretch and release technique for removal (15cmX20cm)

Adhesive, Transparent film Dressing with window frame delivery style, Waterproof, sterile, Bacterial and viral barrier, high adhesive but skin friendly with easy stretch and release technique for removal (5cmX5.7cm)

Adhesive, Transparent IV Dressing with window frame delivery style, Waterproof, sterile, Bacterial and viral barrier, high adhesive but skin friendly with easy stretch and release technique for removal (10cmX12cm)

Adhesive, Transparent IV dressing with window frame delivery style, Waterproof, sterile, Bacterial and viral barrier, high adhesive but skin friendly with easy stretch and release technique for removal (6cmx7cm)

Adhesive, Transparent Polyethylene Surgical Tape : perforated, breathable, polyethylene, transparent backing with straight and easy bi-directional tear, coated with pressure sensitive, Hypoallergenic Acrylate with high adhesive strength Tape 1.25cmx9.14m

Adhesive, Transparent Polyethylene Surgical Tape : perforated, breathable, polyethylene, transparent backing with straight and easy bi-directional tear, coated with pressure sensitive, Hypoallergenic Acrylate with high adhesive strength Tape 2.5cmx9.14m

Adhesive, Transparent Polyethylene Surgical Tape : perforated, breathable, polyethylene, transparent backing with straight and easy bi-directional tear, coated with pressure sensitive, Hypoallergenic Acrylate with high adhesive strength Tape 5cmx9.14m

Adhesive, Transparent polyethylene Surgical Tape : perforated, breathable, polyethylene, transparent backing with straight and easy bi-directional tear, coated with pressure sensitive, Hypoallergenic Acrylate with high adhesive strength Tape 7.5cmx9.14m

Adhesive, Transparent sterile water proof, bacterial and viral barrier polyurethane film with absorbent non-adherent pad and hypoallergenic acrylic adhesive’ with window frame delivery style, (6cmX10cm)

Adhesive, Transparent sterile water proof, bacterial and viral barrier polyurethane film with absorbent non-adherent pad and hypoallergenic acrylic adhesive’ with window frame delivery style, (9cmX10cm)

Adhesive, Transparent sterile water proof, bacterial and viral barrier polyurethane film with absorbent non-adherent pad and hypoallergenic acrylic adhesive’ with window frame delivery style, (9cmX15cm)

Adhesive, Transparent sterile water proof, bacterial and viral barrier polyurethane film with absorbent non-adherent pad and hypoallergenic acrylic adhesive’ with window frame delivery style, (9cmX20cm)

AMBU Bag (Resuscitation Bags)- 240ml Quantity Technical Specification: 1. Self inflating bag 2. Provided with closed ended reservoir with two valves 3.Face masks: 3 sizes: 00, 01 & 02: 2 of each size per bag making 2 set 4.Its fitted with safety valve set at 40 cm H2O, has an outlet for pressure monitoring 5.Bag should be made of sterilizable synthetic material like silicone 6.Patient valve should be well sealed, have minimum dead space and no forward or backward leaks 7.The bag should have an oxygen inlet which fits into the standard oxygen tubing both from a cylinder and central supply. 8.Reusable face masks should be transparent, fit the patient outlet of the bag easily and have minimum dead space. 9.The system should with stand washing scrubbing and autoclaving procedures, chemical sterilization.

AMBU Bag (Resuscitation Bags)- 500ml Quantity Technical Specification: 1. Self inflating bag 2. Provided with closed ended reservoir with two valves 3.Face masks: 3 sizes: 00, 01 & 02: 2 of each size per bag making 2 set 4.Its fitted with safety valve set at 40 cm H2O, has an outlet for pressure monitoring 5.Bag should be made of sterilizable synthetic material like silicone 6.Patient valve should be well sealed, have minimum dead space and no forward or backward leaks 7.The bag should have an oxygen inlet which fits into the standard oxygen tubing both from a cylinder and central supply. 8.Reusable face masks should be transparent, fit the patient outlet of the bag easily and have minimum dead space. 9.The system should with stand washing scrubbing and autoclaving procedures, chemical sterilization.

Amplatzer extra stiff type guide wire. • Length should be 180 cm & 260cm. • Dia should be 0.038” & 0.035”.

ANTIBIOTIC TULLE DRESSING IMPREGNATED WITH WHITE PARAFFIN WAX 10 X 10 CM

ARTERIAL FILTER (Adult)

Arterial Filter (Pediatric): Polycarbonate , Polyester screen type, FilterPore size 32um , Vent port - female luer port , Priming Volume - 40ml,Max.blood flow rate 2.5L per min.

Arterial Lines : Polyethylene Arterial lines (Single Lumen 18G - Length-10CM/8CM/6CM/4CM) with Seldinger Technique

Arterial Lines : Polyethylene Arterial lines (Single Lumen 20G - Length-10CM/8CM/6CM/4CM) with Seldinger Technique

Arterial Lines : Polyethylene Arterial lines (Single Lumen 22G- Length-10CM/8CM/6CM/4CM) with Seldinger Technique

Bacteria Viral Filters for ventilator Adult size

Bacteria Viral Filters for ventilator Paediatric size

Bag, Colostomy/Ilestomy one-pc transparent bag with oval shaped spiral adhesive including flex zones, hide away outlet and integrated charcoal filter-- custom cut 12-75 mm

BAG, DISPOSABLE, THORACIC DRAINAGE SYSTEM

Bain circuit (adult), Manually adjustable non metallic APL valve for MRI compatibility

Bain circuit (paediatric), Manually adjustable non metallic APL valve for MRI compatibility

Bandage, Crepe Bandage B.P. 10 cmX4 meter

Bandage, Crepe Bandage B.P. 15 cm X 4 meter

Battery Operated Sternal Saw Sysytem Specification :- • All attachment should be made of stainless steel. • Should be fully autoclavable. Reciprocating Saw hand Piece: • Should have sternum guard • Should have minimum 1500 CM • Weight of hand piece with battery should be not more than 3.5 IBS • Saw noise level Should not more than 93 dp • Should be autoclavable except battery • Should be supplied with 2 blades of sternotomy surgery-effective length 34-43 mm, width-1.3mm-9 mm. Saggital Saw handpiece (Redo sternum saw) • The Oscillating saw head should be 360 deg rotatable in eight steps. • Power – More than 220 W • CPM - 0-15,000 • Amplitude - 4˚47 • Weight – Less than 1650 gm including battery & lid • Should be supplied with 2 blades for TJR surgery – Effective Length 85-95mm, Width 19-25mm, Thickness 0.89 – 1.37mm • Should be supplied with 2 blades for General Traumatology – Effective Length 35 – 65 mm, Width 10-50mm, thickness 0.5 – 0.9mm Battery • It should be NiMH/NiCd/Lithium Ion Battery. • The Battery should be of more than 1.7 Ah. Lid • Should have quick locking facility. Sterile Funnel • Should be made of PEEK. Battery Removal Device • For Intra operative removal of Battery. • Should be made of PEEK. Battery Charger • The Battery charger should have 4 charging station. with electronically controlled charging process and automatic switch to maintain the charge. • It automatically should indicate when the battery needs to be replaced. Sterilization Basket • The system should be supplied with perforated basket made of stainless steel. • It should proper holding slots for handpiece & attachment. Sterilization Container • Should be made of aluminum. • The container lid should have reusable PTFE Permanent bacteria filter. The PTFE Bacteria filter last up to 1000 sterilization cycles.

Beaker Glass, Graduated, 1000ml, High-quality Borosilicate Glass that can be heated directly in an open flame

Beaker Glass, Graduated, 250ml, High-quality Borosilicate Glass that can be heated directly in an open flame

Sophisticated Industrial Materials Analytic Labs Pvt. Ltd

Ceg Test House and Research Centre Pvt Ltd

Interstellar Testing Centre Private Limited

STANDARD ANALYTICAL LABORATORY ND PVT LTD

Delhi Test House

DEVANSH TESTING & RESEARCH LABORATORY PVT LTD

Delhi Test House

ITL LABS PVT. LTD

Ceg Test House and Research Centre Pvt Ltd

Interstellar Testing Centre Private Limited