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Ultraflo-R 689

by Innovative Medical Technologies, Inc.

Ultraflo-R 689 is a Class II device made by Innovative Medical Technologies, Inc., listed in FDA GUDID since 13 Feb 2025 (UDI-DI 70857182006509), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number70857182006509 UDI-DI Date13 Feb 2025ListedStatusListed 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  • Withdrawn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-R
Generic name
Blood collection set, invasive
Model / Ref / Catalog
689
Primary DI / UDI-DI
70857182006509
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

Related devices

Category: Blood collection set, invasiveBasic intravenous administration set, invasive

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)