8486621
Ref 8486.621Model 10000201054
8486621 (8486.621) is a Class I device made by Richard Wolf GmbH, registered in EUDAMED on 1 Sep 2026 (Basic UDI-DI B-04055207017692) and listed in FDA GUDID since 12 Aug 2022 (UDI-DI 04055207017692), active as of 24 Oct 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-04055207017692 04055207017692 | Date1 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04055207017692 | Date12 Aug 2022 | StatusListed |
Official records
- EUDAMED public site B-04055207017692
- AccessGUDID record 04055207017692
Across registries
- EUDAMED Basic UDI-DI B-04055207017692 registered 1 Sep 2026 Active
- FDA GUDID UDI-DI 04055207017692 listed 12 Aug 2022 Listed
Timeline
- Listed FDA GUDID 04055207017692
- Registered EUDAMED B-04055207017692
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Rigid endoscopic tissue manipulation forceps, reusable
- Device name
- Arthroscopic forceps
- Model / Ref / Catalog
- 10000201054, 8486.621, 8486621
- Description
- MINIATURE GRASPING FORCEPS Ø 2MM jaw straight, sheath straight, WL 60mm, reusable
- Primary DI / UDI-DI
- 04055207017692
- Basic UDI-DI
- B-04055207017692
- FDA product code
- NBH
- EMDN code
- L1904 Arthroscopic surgery forceps and punches, reusable
- GMDN term
- Rigid endoscopic tissue manipulation forceps, reusable
- Device class
- Class I
- Regulation number
- 888.1100
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- Size
- Outer Diameter — 2 Millimeter
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | 10000201054 8486.621 | 8486621 |
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