6250-65-30
by Zimmer, Inc.
Ref 00-6250-065-30
6250-65-30 (00-6250-065-30) is a device classified as Class IIb in the EU and Class II in the US made by Zimmer, Inc., registered in EUDAMED on 1 Nov 2026 (Basic UDI-DI B-00889024119826) and listed in FDA GUDID since 24 Nov 2017 (UDI-DI 00889024119826), 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-00889024119826 00889024119826 | Date1 Nov 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00889024119826 | Date24 Nov 2017 | StatusListed |
Official records
- EUDAMED public site B-00889024119826
- AccessGUDID record 00889024119826
Across registries
- EUDAMED Basic UDI-DI B-00889024119826 registered 1 Nov 2026 Active
- FDA GUDID UDI-DI 00889024119826 listed 24 Nov 2017 Listed
Timeline
- Listed FDA GUDID 00889024119826
- Registered EUDAMED B-00889024119826
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Orthopaedic bone screw, non-bioabsorbable, sterile
- Device name
- HP Acetabular Screws_ BONE SCREW 6.5 Implants
- Model / Ref / Catalog
- 00-6250-065-30, 6250-65-30
- Primary DI / UDI-DI
- 00889024119826
- Basic UDI-DI
- B-00889024119826
- FDA product code
- LPH
- EMDN code
- P09088099 Hip prostheses - other accessories
- GMDN term
- Orthopaedic bone screw, non-bioabsorbable, sterile
- Device class
- Class IIb EUDAMEDClass II GUDID
- Regulation number
- 888.3358
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 30 Millimeter
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | 00-6250-065-30 | 6250-65-30 |
| Device class | Class IIb | Class II |
| Implantable | Yes | No |
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