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Ultraflo-Pb 7391

by Innovative Medical Technologies, Inc.

Ultraflo-Pb 7391 is a Class II device made by Innovative Medical Technologies, Inc., listed in FDA GUDID since 11 Jun 2026 (UDI-DI 00850085666352), 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 Number00850085666352 UDI-DI Date11 Jun 2026ListedStatusListed 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  • Withdrawn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
Ultraflo-Pb
Generic name
Blood collection set, invasive
Model / Ref / Catalog
7391
Primary DI / UDI-DI
00850085666352
FDA product code
FPA, JKA
GMDN term
Blood collection set, invasive
Device class
Class II
Regulation number
880.5440, 862.1675
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Other devices from Innovative Medical Technologies, Inc.

See all devices from Innovative Medical Technologies, Inc. →

Properties

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