Kmi Imi Group Sfrt
Kmi Imi Group Sfrt is a Class I device made by Innovative Med, Inc., listed in FDA GUDID since 3 Jul 2017 (UDI-DI 00851314007205), 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 | Number00851314007205 | Date3 Jul 2017 | StatusListed |
Official records
- AccessGUDID record 00851314007205
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Kmi Imi Group
- Generic name
- Surgical irrigation/aspiration tubing set
- Model / reference
- SFRT
- Primary DI / UDI-DI
- 00851314007205
- FDA product code
- KGZ
- GMDN term
- Surgical irrigation/aspiration tubing set
- Device class
- Class I
- Regulation number
- 878.4200
- GUDID distribution status
- In Commercial Distribution
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