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Pmi PMI250ML

by Progressive Medical, Inc.

Pmi PMI250ML is a Class II device made by Progressive Medical, Inc., listed in FDA GUDID since 1 May 2018 (UDI-DI 00812608021642), 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 Number00812608021642 UDI-DI Date1 May 2018ListedStatusListed 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  • Withdrawn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
Fluid transfer set, general-purpose
Model / Ref / Catalog
PMI250ML
Primary DI / UDI-DI
00812608021642
FDA product code
KPE
GMDN term
Fluid transfer set, general-purpose
Device class
Class II
Regulation number
880.5025
GUDID distribution status
In Commercial Distribution
Size
Total Volume — 250 Milliliter

Related devices

Category: Fluid transfer set, general-purpose

Similar devices in this category

Other devices filed under Fluid transfer set, general-purpose.

Other devices from Progressive Medical, Inc.

See all devices from Progressive Medical, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)