Diamedix 720-600
Diamedix 720-600 is a Class I device made by Diamedix Corp., listed in FDA GUDID since 20 Sep 2016 (UDI-DI 00817273020310), 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 | Number00817273020310 | Date20 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 00817273020310
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Diamedix
- Generic name
- Cryptosporidium parvum immunoglobulin G (IgG) antibody IVD, kit, immunoblot
- Model / reference
- 720-600
- Description
- "720-600 EBV-VCA IgG Test Kit"
- Primary DI / UDI-DI
- 00817273020310
- FDA product code
- LJY
- GMDN term
- Cryptosporidium parvum immunoglobulin G (IgG) antibody IVD, kit, immunoblot
- Device class
- Class I
- Regulation number
- 866.3380
- GUDID distribution status
- In Commercial Distribution
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- Anti-Mumps Virus AT ELISA (IgG) EI 2630-9601-3 G by EUROIMMUN Medizinische Labordiagnostika AG