Coag Dissector 165 cm
Coag Dissector 165 cm (200.50) is a Class II device made by Ovesco Endoscopy AG, cleared under FDA 510(k) K141794 on 19 Nov 2014 and listed in FDA GUDID since 5 Jul 2018 (UDI-DI 04260206311027), 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 | Number04260206311027 | Date5 Jul 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK141794 | Date19 Nov 2014 | StatusActive |
Official records
- AccessGUDID record 04260206311027
- FDA 510(k) database K141794
Across registries
- FDA 510(k) K141794 decided 19 Nov 2014 Active
- FDA GUDID UDI-DI 04260206311027 listed 5 Jul 2018 Listed
Timeline
- Cleared FDA 510(k) K141794
- Listed FDA GUDID 04260206311027
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Coag Dissector
- Generic name
- Endoscopic electrosurgical handpiece/electrode, monopolar, single-use
- Model / Ref / Catalog
- 165 cm, 200.50
- Primary DI / UDI-DI
- 04260206311027
- 510(k) Number
- FDA product code
- KGE
- GMDN term
- Endoscopic electrosurgical handpiece/electrode, monopolar, single-use
- Device class
- Class II
- Regulation number
- 876.4300
- GUDID distribution status
- In Commercial Distribution
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