Erbe 20193-072
Erbe 20193-072 is a Class II device made by Erbe Elektromedizin GmbH, cleared under FDA 510(k) K972269 on 9 Jul 1997 and listed in FDA GUDID since 16 Dec 2016 (UDI-DI 04050147005143), 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 | Number04050147005143 | Date16 Dec 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK972269 | Date9 Jul 1997 | StatusActive |
Official records
- AccessGUDID record 04050147005143
- FDA 510(k) database K972269
Across registries
- FDA 510(k) K972269 decided 9 Jul 1997 Active
- FDA GUDID UDI-DI 04050147005143 listed 16 Dec 2016 Listed
Timeline
- Cleared FDA 510(k) K972269
- Listed FDA GUDID 04050147005143
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Erbe
- Generic name
- Electrosurgical return electrode, single-use
- Model / Ref / Catalog
- 20193-072
- Primary DI / UDI-DI
- 04050147005143
- 510(k) Number
- FDA product code
- GEI
- GMDN term
- Electrosurgical return electrode, single-use
- Device class
- Class II
- Regulation number
- 878.4400
- GUDID distribution status
- In Commercial Distribution
- Size
- Area/Surface Area — 136.000 Square centimeter
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