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Polypropylene monofilament Suture size 4-0 , 19 mm needle 70 cm 3 by 8 circle Round cutting (SYNTHALIN)(19 mm needle 70 cm 3 by 8 circle round cutting)

` 108.00

  • MRP: `190.00

3/8 Circle Round cutting , 19 mm x 70 cm suture is most widely used braided and coated synthetic absorbable suture in the world. On account of its superior properties, this suture has replaced catgut sutures in most applications. Polyglactin 910 suture is a synthetic absorbable sterile surgicasuture composed of a copolymer made from 90 Glycolide and 10 L-lactide..

  • Availability: 10,000 In Stock
  • Min. Qty. Per Consignee: 60
  • category of suture - Non absorbable
  • Construction - Monofilament
  • Suture Material - Polypropylene
  • Coating Material - wax
  • Needle Length - 20 mm
Other Specifications Download Specification
Governing Specification USP 39
Category Of Suture Non absorbable
Construction Monofilament
Suture Material Polypropylene
Coating with coating
Coating Material wax
Number Of Strands 1
Suture Length 70 cm
Needle Length 20 mm
Type Of Needles Round bodied
Needle Curvature 3/8 circle
If Others Then Declare Nil
Sterilised yes
Sterilisation Method Ethylene Oxide
Shelf Life 5 year
No. Of Sutures In A Pack 12
Sutures Confirming To Provisions Of Drug And Cosmetic Act YES
Date Of Drug Licence 30/04/2016
Whether Drug License Valid YES
Date Of Non Conviction Certificate 29/10/2016
To Indicate Whether Holding RGMP Issued Under Revised Schedule-`M' Of Drugs & Cosmetics Act 1940 As Amended Or WHO-GMP(for Manufacturers Only) As Per Norms Amended Up To Date Issued By Licensing Authority Or Other Certifications In Respect Of The OEM. yes
Packing As Per Drug Act Provisions And USP YES
Each Packing Shall Be Marked As Under:-a. Nomenclature Of The Stores B. Manufacturers Name, Address, C. Drug License No., D. Month Of Manufacturing, E. Expiry F. Batch No And Lot No (if Applicable) G. Any Other Particulars Required Under Drug Act 1940 Amended Up To Date H. Quantity Contained Therein I. Manufacturers Name Or Trade Mark, YES
Copies Of In House Test Report To Be Forwarded With Each Supply YES
Cartons Shall Be Marked With Manufacturers Name, Batch No And Month Of Manufacture And Use Before. If Indentor Specifies Any Special Marking In Supply Order (eg.CGHS, Railways, CRPF Etc) Same Shall Be Provided. YES
All Packs Must Indicate The Date Of Manufacture And Expiry. In Addition All Supplies Shall Have A Remaining Self Life Of At Least Three - Fourth (3/4th) Of The Stipulated Shelf Life At The Time Of Delivery. YES
If Any Batch Must Be Recalled Because Of Problems With Product Quality Or Adverse Reactions To The Item, The Supplier Will Be Responsible To Notify The Purchaser,reactions To The Item, The Supplier Will Be Responsible To Notify The Purchaser,providing Full Details About The Reason Leading To The Recall And Shall Take Steps To Replace The Product In Question At Its Own Cost With A Fresh Batch Of Acceptable Quality Or Withdraw And Give A Full Refund Of The Value Batch Has Been Taken Off The Market Due To Safety Problems. YES
Test Report From Drug Controller Approved Laboratories Available YES
Test Report Number B7003
Date Of Issue Of Test Report By Laboratory 23/08/2017
Name And Address Of Laboratory Sri Orion pharmaceuticals & sutures , No. 138-B, 3rd floor,KIADB Industrial Area, Peenya, Bengaluru - 560058, Karnataka
Whether Non Conviction Certificate Issued By Drug Authorities Available YES

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