Diamedix 720-850
Diamedix 720-850 is a Class I device made by Diamedix Corp., listed in FDA GUDID since 20 Sep 2016 (UDI-DI 00817273020419), 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 | Number00817273020419 | Date20 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 00817273020419
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Diamedix
- Generic name
- Echinococcus granulosus/E. multilocularis immunoglobulin G (IgG) antibody IVD, control
- Model / reference
- 720-850
- Description
- "720-850 Mycoplasma IgG Test Kit"
- Primary DI / UDI-DI
- 00817273020419
- FDA product code
- LJZ
- GMDN term
- Echinococcus granulosus/E. multilocularis immunoglobulin G (IgG) antibody IVD, control
- Device class
- Class I
- Regulation number
- 866.3375
- GUDID distribution status
- In Commercial Distribution
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