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nonabsorbable surgical sutures, os 5333, size 2-0, length 76cm, 30 mm needle, box of 12 foils (sriorion by tarck)(os 5333)

` 642.00

  • MRP: `1284.00

NONABSORBABLE SURGICAL SUTURES, OS 5333, SIZE 2-0, LENGTH 76cm, 30 mm needle, BOX OF 12 FOILS.

  • Availability: 100,000 In Stock
  • Min. Qty. Per Consignee: 10
  • category of suture - Non absorbable
  • Construction - Monofilament
  • Suture Material - Black Braided Silk
  • Coating Material - BLACK BRAIDED SILK
  • Needle Length - 30 mm
Other Specifications Download Specification
Governing Specification USP 39
Category Of Suture Non absorbable
Construction Monofilament
Suture Material Black Braided Silk
Coating with coating
Coating Material BLACK BRAIDED SILK
Number Of Strands 1
Suture Length 76 cm
Needle Length 30 mm
Type Of Needles Round bodied
Needle Curvature 1/2 circle
If Others Then Declare NA
Sterilised yes
Sterilisation Method ethylene oxide
Shelf Life 5
No. Of Sutures In A Pack 12
Sutures Confirming To Provisions Of Drug And Cosmetic Act YES
Date Of Drug Licence Drug License No. KTK/28/268/94, Dated 30.04.2016, Valid till 29.04.2021
Whether Drug License Valid YES
Date Of Non Conviction Certificate NA
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. GME Certificate No. DCD/CR -448/SPL.CELL-1/2017-18 dated 27.11.2017 Valid till 26.11.2018
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 B7042
Date Of Issue Of Test Report By Laboratory 23/11/2017
Name And Address Of Laboratory SRI ORION PHARMACEUTICALS & SUTURES, 138/B UDAYAGIRI COMPLEX 3rd PHASE, KIADB INDUSTRIAL AREA, PEENYA, BANGALORE-560058 (INDIA)
Whether Non Conviction Certificate Issued By Drug Authorities Available YES

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