gi4000
gi4000 (G1110001) is a Class II device made by US Endoscopy, listed in FDA GUDID since 18 Feb 2022 (UDI-DI 00724995180256), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00724995180256 | Date18 Feb 2022 | StatusListed |
Official records
- AccessGUDID record 00724995180256
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Inert gas-enhanced electrosurgical system
- Model / Ref / Catalog
- gi4000, G1110001
- Primary DI / UDI-DI
- 00724995180256
- FDA product code
- GEI, FEQ
- GMDN term
- Inert gas-enhanced electrosurgical system
- Device class
- Class II
- Regulation number
- 878.4400, 876.1500
- GUDID distribution status
- In Commercial Distribution
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