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chromic 2.0 (chromic)(20)

` 130.00

  • MRP: `150.00

2.0.

  • Availability: 13 In Stock
  • Min. Qty. Per Consignee: 10
  • category of suture - absorbabale
  • Construction - Monofilament
  • Suture Material - Black Braided Silk
  • Coating Material - Wax
  • Needle Length - 45 mm
Other Specifications Download Specification
Governing Specification USP 39
Category Of Suture absorbabale
Construction Monofilament
Suture Material Black Braided Silk
Coating with coating
Coating Material Wax
Number Of Strands 1
Suture Length 45 cm
Needle Length 45 mm
Type Of Needles Not Applicable
Needle Curvature 1/2 circle
If Others Then Declare Nil
Sterilised yes
Sterilisation Method Ethylene Oxide
Shelf Life 12
No. Of Sutures In A Pack 6
Sutures Confirming To Provisions Of Drug And Cosmetic Act YES
Date Of Drug Licence 24.04.2016
Whether Drug License Valid YES
Date Of Non Conviction Certificate 21.12.2017
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. DCD/CR-445/SPL.Cell-1/2016-2017
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 B7007
Date Of Issue Of Test Report By Laboratory 25/08/2017
Name And Address Of Laboratory SRI ORION PHARMACEUTICALS & SUTURES , No. 138-B, 3rd floor, Udayagiri complex, 3rd Phase, KIADB Industrial Area, Peenya, Bengaluru
Whether Non Conviction Certificate Issued By Drug Authorities Available YES

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