Deknatel IPN927811
Deknatel IPN927811 (D-7070M4K) is a Class II device made by Teleflex Incorporated, listed in FDA GUDID since 31 Jul 2023 (UDI-DI 14026704730152), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number14026704730152 | Date31 Jul 2023 | StatusListed |
Official records
- AccessGUDID record 14026704730152
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Deknatel
- Generic name
- Polyolefin/fluoropolymer suture, monofilament
- Model / Ref / Catalog
- IPN927811, D-7070M4K
- Primary DI / UDI-DI
- 14026704730152
- FDA product code
- GAW
- GMDN term
- Polyolefin/fluoropolymer suture, monofilament
- Device class
- Class II
- Regulation number
- 878.5010
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Safe
- Size
- Length — 75 Centimeter
Similar devices in this category
Other devices filed under Polyolefin/fluoropolymer suture, monofilament.
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- FSSB A003PP by Surgical Specialties México, S. de R.L. de C.V.
- Biotex BT5019 by PURGO BIOLOGICS Inc.
- GORE-TEX Suture 6K08 by W. L. Gore & Associates, Inc.
- FILBLOC PERMANENT PLY-G02-020-A by ASSUT EUROPE SPA