Deknatel IPN923602
Ref EGFS-1A
Deknatel IPN923602 (EGFS-1A) is a Class I device made by Teleflex Incorporated, registered in EUDAMED on 6 Aug 2026 (Basic UDI-DI 08019020000000000000156KQ) and listed in FDA GUDID since 4 Sep 2025 (UDI-DI 14026704738981), active as of 24 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number08019020000000000000156KQ 14026704738981 | Date6 Aug 2026 | StatusActive |
| United States | GUDID listing GUDID | Number14026704738981 | Date4 Sep 2025 | StatusListed |
Official records
- EUDAMED public site 08019020000000000000156KQ
- AccessGUDID record 14026704738981
Across registries
- EUDAMED Basic UDI-DI 08019020000000000000156KQ registered 6 Aug 2026 Active
- FDA GUDID UDI-DI 14026704738981 listed 4 Sep 2025 Listed
Timeline
- Listed FDA GUDID 14026704738981
- Registered EUDAMED 08019020000000000000156KQ
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Gabbay-Frater Sutorganizer (4 Pieces of 1) EUDAMEDDeknatel GUDID
- Generic name
- Polyester suture, non-bioabsorbable, multifilament, non-antimicrobial
- Device name
- Gabbay-Frater Suture Guide
- Model / Ref / Catalog
- EGFS-1A, IPN923602
- Primary DI / UDI-DI
- 14026704738981
- Basic UDI-DI
- 08019020000000000000156KQ
- FDA product code
- FZK
- EMDN code
- H9099 Suture devices - other
- GMDN term
- Polyester suture, non-bioabsorbable, multifilament, non-antimicrobial
- Device class
- Class I
- Regulation number
- 878.4950
- EU registration type
- Standard device
- EU market of registration
- Ireland
- GUDID distribution status
- In Commercial Distribution
- Size
- Depth — 0.75 InchLength — 9 InchWidth — 1.5 Inch
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | EGFS-1A | IPN923602 |
| Implantable | No | Yes |
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