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Pmi PMIX03

by Progressive Medical, Inc.

Pmi PMIX03 is a Class II device made by Progressive Medical, Inc., listed in FDA GUDID since 18 Mar 2019 (UDI-DI 00812608022007), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00812608022007 UDI-DI Date18 Mar 2019ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Pmi
Generic name
Compounding transfer set
Model / Ref / Catalog
PMIX03
Primary DI / UDI-DI
00812608022007
FDA product code
FPA
GMDN term
Compounding transfer set
Device class
Class II
Regulation number
880.5440
GUDID distribution status
In Commercial Distribution

Related devices

Category: Compounding transfer set

Similar devices

Other devices filed under FDA product code FPA (Set, Administration, Intravascular).

Other devices from Progressive Medical, Inc.

See all devices from Progressive Medical, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)