Instruments
Ref 03.333.017
Active
CE MDR
Valid until
Not listed
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number019644901457 00196449024230 | Date12 Mar 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00196449024230 | Date24 Jul 2025 | StatusListed |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade Name
- Cannulated Headless Screw - Full Thread
- Generic Name
- Orthopaedic guidewire, single-use
- Device Name
- Instruments
- Model / Reference
- 03.333.017
- Primary DI / UDI-DI
- 00196449024230
- Basic UDI-DI
- 019644901457
- FDA Product Code
- LXH
- EMDN Code
- L0922 Orthopaedic surgery guides, reusable
- GMDN Term
- Orthopaedic guidewire, single-use
- Device Class
- Class IIa EUDAMEDClass I GUDID
- Regulation Number
- 888.4540
- EU market of registration
- Belgium
- GUDID distribution status
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device Class | Class IIa | Class I |
Manufacturer details
- EUDAMED SRN
- US-MF-000011350
- Authorised representative
- MDSS GmbH DE-AR-000005430
Other devices from Tyber Medical
Properties
Other properties (19)
- Sterile: No
- Implantable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Serial Number: No
- Expiration Date: No
- Manufacturing Date: No