Lumex 89220
Lumex 89220 is a Class I device made by GF Health Products, Inc., listed in FDA GUDID since 8 Jan 2021 (UDI-DI M368892201), registry data as of 8 Nov 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | NumberM368892201 | Date8 Jan 2021 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Lumex
- Generic name
- Commode, manual
- Model / Ref / Catalog
- 89220
- Primary DI / UDI-DI
- M368892201
- FDA product code
- INM
- GMDN term
- Commode, manual
- Device class
- Class I
- Regulation number
- 890.3100
- GUDID distribution status
- In Commercial Distribution
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