M7 F9000290
by Asa SRL
M7 F9000290 is a Class II device made by Asa SRL, listed in FDA GUDID since 21 Nov 2023 (UDI-DI 08033765391689), registry data as of 23 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 | Number08033765391689 | Date21 Nov 2023 | StatusListed |
Official records
- AccessGUDID record 08033765391689
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- M7
- Generic name
- Musculoskeletal infrared phototherapy unit, non-wearable
- Model / reference
- F9000290
- Primary DI / UDI-DI
- 08033765391689
- FDA product code
- ILY
- GMDN term
- Musculoskeletal infrared phototherapy unit, non-wearable
- Device class
- Class II
- Regulation number
- 890.5500
- GUDID distribution status
- In Commercial Distribution
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