125300
Ref 125300
125300 is a Class I device made by Karl Storz SE & CO. KG, registered in EUDAMED on 19 May 2026 (Basic UDI-DI 4048551000326TD) and listed in FDA GUDID since 23 Feb 2019 (UDI-DI 04048551054413), 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 | Number4048551000326TD 04048551054413 | Date19 May 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04048551054413 | Date23 Feb 2019 | StatusListed |
Official records
- EUDAMED public site 4048551000326TD
- AccessGUDID record 04048551054413
Across registries
- EUDAMED Basic UDI-DI 4048551000326TD registered 19 May 2026 Active
- FDA GUDID UDI-DI 04048551054413 listed 23 Feb 2019 Listed
Timeline
- Listed FDA GUDID 04048551054413
- Registered EUDAMED 4048551000326TD
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Tuning fork
- Device name
- Tuning forks, metal
- Model / reference
- 125300
- Primary DI / UDI-DI
- 04048551054413
- Basic UDI-DI
- 4048551000326TD
- FDA product code
- LRC
- EMDN code
- L140599 Ear surgery instruments, reusable - other
- GMDN term
- Tuning fork
- Device class
- Class I
- Regulation number
- 874.4420
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Similar devices in this category
Other devices filed under EAR SURGERY INSTRUMENTS, REUSABLE - OTHER.