LigaSure MRASILF19
by Covidien LP
LigaSure MRASILF19 is a Class II device made by Covidien LP, cleared under FDA 510(k) K261070 on 15 Sep 2026 and listed in FDA GUDID since 23 Oct 2026 (UDI-DI 10884521783829), active as of 9 Nov 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 | Number10884521783829 | Date23 Oct 2026 | StatusListed |
| United States | FDA 510(k)SESE | NumberK261070 | Date15 Sep 2026 | StatusActive |
Official records
- AccessGUDID record 10884521783829
- FDA 510(k) database K261070
Across registries
- FDA 510(k) K261070 decided 15 Sep 2026 Active
- FDA GUDID UDI-DI 10884521783829 listed 23 Oct 2026 Listed
Timeline
- Cleared FDA 510(k) K261070
- Listed FDA GUDID 10884521783829
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- LigaSure
- Generic name
- Robotic endoscopic electrosurgical instrument, bipolar, single-use
- Model / reference
- MRASILF19
- Primary DI / UDI-DI
- 10884521783829
- 510(k) Number
- FDA product code
- GEI
- GMDN term
- Robotic endoscopic electrosurgical instrument, bipolar, single-use
- Device class
- Class II
- Regulation number
- 878.4400
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 44 CentimeterOuter Diameter — 5 Millimeter