Pmi PMIX01
Pmi PMIX01 is a Class II device made by Progressive Medical, Inc., listed in FDA GUDID since 18 Mar 2019 (UDI-DI 00812608021963), 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 | Number00812608021963 | Date18 Mar 2019 | StatusListed |
Official records
- AccessGUDID record 00812608021963
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Pmi
- Generic name
- Compounding transfer set
- Model / Ref / Catalog
- PMIX01
- Primary DI / UDI-DI
- 00812608021963
- FDA product code
- FPA
- GMDN term
- Compounding transfer set
- Device class
- Class II
- Regulation number
- 880.5440
- GUDID distribution status
- In Commercial Distribution
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