Onatec OB468555
by Surgical Specialties México, S. de R.L. de C.V.
Ref OB468555Model Polyester Sutures
Onatec OB468555 is a device classified as Class III 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-00848782006175) and listed in FDA GUDID since 26 Apr 2022 (UDI-DI 00848782006175), 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-00848782006175 00848782006175 | Date29 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00848782006175 | Date26 Apr 2022 | StatusListed |
Official records
- EUDAMED public site B-00848782006175
- AccessGUDID record 00848782006175
Across registries
- EUDAMED Basic UDI-DI B-00848782006175 registered 29 Oct 2026 Active
- FDA GUDID UDI-DI 00848782006175 listed 26 Apr 2022 Listed
Timeline
- Listed FDA GUDID 00848782006175
- Registered EUDAMED B-00848782006175
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Onabond EUDAMEDOnatec GUDID
- Generic name
- Polyester suture, non-bioabsorbable, multifilament, non-antimicrobial
- Model / Ref / Catalog
- OB468555, Polyester Sutures
- Primary DI / UDI-DI
- 00848782006175
- Basic UDI-DI
- B-00848782006175
- FDA product code
- GAT
- EMDN code
- H010201010201 Polyester and derivatives monofilament with needle
- GMDN term
- Polyester suture, non-bioabsorbable, multifilament, non-antimicrobial
- Device class
- Class III EUDAMEDClass II GUDID
- Regulation number
- 878.5000
- 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 III | Class II |
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