Non-Locking Screw 1312-20-522
Ref 131220522
Non-Locking Screw 1312-20-522 (131220522) is a device classified as Class IIb in the EU and Class II in the US made by Biomet Orthopedics, Inc., registered in EUDAMED on 24 Oct 2026 (Basic UDI-DI B-00887868547867) and listed in FDA GUDID since 15 Nov 2022 (UDI-DI 00887868547867), 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-00887868547867 00887868547867 | Date24 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00887868547867 | Date15 Nov 2022 | StatusListed |
Official records
- EUDAMED public site B-00887868547867
- AccessGUDID record 00887868547867
Across registries
- EUDAMED Basic UDI-DI B-00887868547867 registered 24 Oct 2026 Active
- FDA GUDID UDI-DI 00887868547867 listed 15 Nov 2022 Listed
Timeline
- Listed FDA GUDID 00887868547867
- Registered EUDAMED B-00887868547867
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Non-Locking Screw
- Generic name
- Orthopaedic bone screw, non-bioabsorbable, non-sterile
- Device name
- Anatomic 1_5mm cortical nonlocking screw
- Model / Ref / Catalog
- 131220522, 1312-20-522
- Primary DI / UDI-DI
- 00887868547867
- Basic UDI-DI
- B-00887868547867
- FDA product code
- HTY, KTT, LXT, HSB, HTN, HWC, JDW, HRS
- EMDN code
- P09120601 Cortical screws
- GMDN term
- Orthopaedic bone screw, non-bioabsorbable, non-sterile
- Device class
- Class IIb EUDAMEDClass II GUDID
- Regulation number
- 888.3040, 888.3030, 888.3020
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | 131220522 | 1312-20-522 |
| Device class | Class IIb | Class II |
| Implantable | Yes | No |
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