Erbe 20150-300
Erbe 20150-300 is a Class II device made by Erbe Elektromedizin GmbH, cleared under FDA 510(k) K072404 on 31 Oct 2007 and listed in FDA GUDID since 11 Oct 2016 (UDI-DI 04050147001930), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number04050147001930 | Date11 Oct 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK072404 | Date31 Oct 2007 | StatusActive |
Official records
- AccessGUDID record 04050147001930
- FDA 510(k) database K072404
Across registries
- FDA 510(k) K072404 decided 31 Oct 2007 Active
- FDA GUDID UDI-DI 04050147001930 listed 11 Oct 2016 Listed
Timeline
- Cleared FDA 510(k) K072404
- Listed FDA GUDID 04050147001930
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Erbe
- Generic name
- Water jet knife system pump-cartridge
- Model / Ref / Catalog
- 20150-300
- Primary DI / UDI-DI
- 04050147001930
- 510(k) Number
- FDA product code
- FQH
- GMDN term
- Water jet knife system pump-cartridge
- Device class
- Class II
- Regulation number
- 880.5475
- GUDID distribution status
- In Commercial Distribution
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