Triax 5150-9-946
Ref 5150-9-946Model 08858251002938TQ
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 | Number08858251002938TQ 07613327093360 | Date16 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number07613327093360 | Date24 Sep 2020 | 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- Withdrawn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
- Triax
- Generic Name
- Instrument tray, reusable
- Device Name
- Monotube Triax - Trays and Tray Accessories - Class I - Non Sterile
- Model / Ref / Catalog
- 5150-9-946, 08858251002938TQ
- Description
- Storage Case Blue , Red
- Primary DI / UDI-DI
- 07613327093360
- Basic UDI-DI
- 08858251002938TQ
- Direct Marketing DI
- 07613327093360
- FDA Product Code
- LXH
- EMDN Code
- P09120499 External bone fixation systems - other
- GMDN Term
- Instrument tray, reusable
- Device Class
- Class I
- Regulation Number
- 888.4540
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Other devices from Stryker Corp.
Properties
Other properties (21)
- Sterile: No
- Single Use: No
- Implantable: No
- Reusable: 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