Phoenix Diagnostics, Inc. PH7000
Phoenix Diagnostics, Inc. PH7000 is a Class II device made by Phoenix Diagnostics, Inc., listed in FDA GUDID since 26 Jan 2018 (UDI-DI 00853366007448), 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 | Number00853366007448 | Date26 Jan 2018 | StatusListed |
Official records
- AccessGUDID record 00853366007448
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Phoenix Diagnostics, Inc.
- Generic name
- Multiple-type clinical chemistry analyte profile IVD, calibrator
- Model / reference
- PH7000
- Primary DI / UDI-DI
- 00853366007448
- FDA product code
- JIX
- GMDN term
- Multiple-type clinical chemistry analyte profile IVD, calibrator
- Device class
- Class II
- Regulation number
- 862.1150
- GUDID distribution status
- In Commercial Distribution
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