Diamedix MAGO Plus
Diamedix MAGO Plus is a Class I device made by Diamedix Corp., listed in FDA GUDID since 21 Sep 2016 (UDI-DI 00817273020464), 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 | Number00817273020464 | Date21 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 00817273020464
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Diamedix
- Generic name
- Multichannel clinical chemistry analyser IVD, point-of-care, line-powered
- Model / reference
- MAGO Plus
- Primary DI / UDI-DI
- 00817273020464
- FDA product code
- JJF
- GMDN term
- Multichannel clinical chemistry analyser IVD, point-of-care, line-powered
- Device class
- Class I
- Regulation number
- 862.2170
- GUDID distribution status
- In Commercial Distribution
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