Deknatel IPN012610
Listed
Valid until
Not applicable
FDA recalls
None ongoingDocuments
None
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number04026704423651 | Date16 Oct 2015 | StatusListed |
Recalls
-
- Terminated Z-1017-2007
Suture Diameter/Strength specification failure: The products may not meet their final specifications for suture diameter and/or strength which could lead to premature breakage.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- Deknatel
- Generic Name
- Polyester suture, non-bioabsorbable, multifilament, non-antimicrobial
- Model / Ref / Catalog
- IPN012610, G7-113C9K
- Primary DI / UDI-DI
- 04026704423651
- 510(k) Number
- FDA Product Code
- GAT
- GMDN Term
- Polyester suture, non-bioabsorbable, multifilament, non-antimicrobial
- Device Class
- Class II
- Regulation Number
- 878.5000
- GUDID distribution status
- In Commercial Distribution
- MRI Safety
- MR Safe
- Size
- Length — 75 Centimeter
Other devices from Teleflex Incorporated
Properties
Other properties (8)
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Manufacturing Date: No