174700
Ref 174700
174700 is a Class I device made by Karl Storz SE & CO. KG, registered in EUDAMED on 19 May 2026 (Basic UDI-DI 4048551000363TK) and listed in FDA GUDID since 4 Sep 2018 (UDI-DI 04048551058534), 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 | Number4048551000363TK 04048551058534 | Date19 May 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04048551058534 | Date4 Sep 2018 | StatusListed |
Official records
- EUDAMED public site 4048551000363TK
- AccessGUDID record 04048551058534
Across registries
- EUDAMED Basic UDI-DI 4048551000363TK registered 19 May 2026 Active
- FDA GUDID UDI-DI 04048551058534 listed 4 Sep 2018 Listed
Timeline
- Listed FDA GUDID 04048551058534
- Registered EUDAMED 4048551000363TK
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Surgical mallet
- Device name
- Mallets, ENT metal, plastics
- Model / reference
- 174700
- Primary DI / UDI-DI
- 04048551058534
- Basic UDI-DI
- 4048551000363TK
- FDA product code
- LRC
- EMDN code
- L149099 ENT instruments, reusable - other
- GMDN term
- Surgical mallet
- 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
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