Onatec OL456295
by Surgical Specialties México, S. de R.L. de C.V.
Ref OL456295Model Nylon Sutures
Onatec OL456295 is a device classified as Class IIb in the EU and Class II in the US made by Surgical Specialties México, S. de R.L. de C.V., registered in EUDAMED on 29 Oct 2026 (Basic UDI-DI B-00848782005970) and listed in FDA GUDID since 25 Apr 2022 (UDI-DI 00848782005970), active as of 7 Nov 2026.
Active
CE MDD
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/MDD EUDAMED | NumberB-00848782005970 00848782005970 | Date29 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00848782005970 | Date25 Apr 2022 | StatusListed |
Official records
- EUDAMED public site B-00848782005970
- AccessGUDID record 00848782005970
Across registries
- EUDAMED Basic UDI-DI B-00848782005970 registered 29 Oct 2026 Active
- FDA GUDID UDI-DI 00848782005970 listed 25 Apr 2022 Listed
Timeline
- Listed FDA GUDID 00848782005970
- Registered EUDAMED B-00848782005970
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Onalon EUDAMEDOnatec GUDID
- Generic name
- Nylon suture, non-bioabsorbable, monofilament
- Model / Ref / Catalog
- OL456295, Nylon Sutures
- Primary DI / UDI-DI
- 00848782005970
- Basic UDI-DI
- B-00848782005970
- FDA product code
- GAR
- EMDN code
- H010201010101 Polyamide monofilament with needle
- GMDN term
- Nylon suture, non-bioabsorbable, monofilament
- Device class
- Class IIb EUDAMEDClass II GUDID
- Regulation number
- 878.5020
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class IIb | Class II |
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