02701000
Ref 02701000Model UMUT16SDSINST
02701000 is a Class I device made by implantcast GmbH, registered in EUDAMED on 28 Aug 2026 (Basic UDI-DI 4048844UMUT16SDSINST8V) and listed in FDA GUDID since 25 Sep 2024 (UDI-DI 04048844150150), active as of 22 Oct 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 | Number4048844UMUT16SDSINST8V 04048844150150 | Date28 Aug 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04048844150150 | Date25 Sep 2024 | StatusListed |
Official records
- EUDAMED public site 4048844UMUT16SDSINST8V
- AccessGUDID record 04048844150150
Across registries
- EUDAMED Basic UDI-DI 4048844UMUT16SDSINST8V registered 28 Aug 2026 Active
- FDA GUDID UDI-DI 04048844150150 listed 25 Sep 2024 Listed
Timeline
- Listed FDA GUDID 04048844150150
- Registered EUDAMED 4048844UMUT16SDSINST8V
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Surgical screwdriver, reusable
- Model / reference
- 02701000, UMUT16SDSINST
- Primary DI / UDI-DI
- 04048844150150
- Basic UDI-DI
- 4048844UMUT16SDSINST8V
- Direct marketing DI
- 04048844150150
- FDA product code
- HXX
- EMDN code
- L26 Surgical screwdrivers, reusable
- GMDN term
- Surgical screwdriver, reusable
- Device class
- Class I
- Regulation number
- 888.4540
- EU registration type
- Standard device
- EU market of registration
- Türkiye
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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