Variax 703928
by Stryker GmbH
Ref 703928Model 08858251002729TD
Variax 703928 is a Class I device made by Stryker GmbH, registered in EUDAMED on 16 Sep 2026 (Basic UDI-DI 08858251002729TD) and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 07613327070149), active as of 12 Nov 2026.
Active
CE MDR
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/MDR EUDAMED | Number08858251002729TD 07613327070149 | Date16 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number07613327070149 | Date24 Sep 2016 | StatusListed |
Official records
- EUDAMED public site 08858251002729TD
- AccessGUDID record 07613327070149
Across registries
- EUDAMED Basic UDI-DI 08858251002729TD registered 16 Sep 2026 Active
- FDA GUDID UDI-DI 07613327070149 listed 24 Sep 2016 Listed
Timeline
- Listed FDA GUDID 07613327070149
- Registered EUDAMED 08858251002729TD
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Variax
- Generic name
- Surgical drill guide, reusable
- Device name
- Variax 2 Instruments - Handles and Adaptors - Class I - Reusable - Non Sterile
- Model / Ref / Catalog
- 703928, 08858251002729TD
- Primary DI / UDI-DI
- 07613327070149
- Basic UDI-DI
- 08858251002729TD
- FDA product code
- LXH
- EMDN code
- P091280 Osteosynthesis devices, devices for tendon and ligament synthesis - accessories
- GMDN term
- Surgical drill guide, reusable
- Device class
- Class I
- Regulation number
- 888.4540
- EU registration type
- Standard device
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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