Erbe 20132-208
Erbe 20132-208 is an inert gas-enhanced electrosurgical handpiece (FDA Class II; FDA product code GEI, Electrosurgical, Cutting & Coagulation & Accessories) made by Erbe Elektromedizin GmbH, cleared under FDA 510(k) K024047 on 8 Jan 2003 and listed in FDA GUDID since 10 Sep 2016 (UDI-DI 04050147014725), 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 | Number04050147014725 | Date10 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK024047 | Date8 Jan 2003 | StatusActive |
Official records
- AccessGUDID record 04050147014725
- FDA 510(k) database K024047
Across registries
- FDA 510(k) K024047 decided 8 Jan 2003 Active
- FDA GUDID UDI-DI 04050147014725 listed 10 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K024047
- Listed FDA GUDID 04050147014725
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Erbe
- Generic name
- Inert gas-enhanced electrosurgical handpiece
- Model / Ref / Catalog
- 20132-208
- Primary DI / UDI-DI
- 04050147014725
- 510(k) Number
- FDA product code
- GEI
- GMDN term
- Inert gas-enhanced electrosurgical handpiece
- Device class
- Class II
- Regulation number
- 878.4400
- GUDID distribution status
- In Commercial Distribution
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