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Ultraflo-A 902

by Innovative Medical Technologies, Inc.

Ultraflo-A 902 is a Class I device made by Innovative Medical Technologies, Inc., listed in FDA GUDID since 14 Feb 2025 (UDI-DI 20857182006290), 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 Number20857182006290 UDI-DI Date14 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  • Withdrawn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-A
Generic name
Blood collection set, noninvasive
Model / Ref / Catalog
902
Primary DI / UDI-DI
20857182006290
FDA product code
KST
GMDN term
Blood collection set, noninvasive
Device class
Class I
Regulation number
864.9125
GUDID distribution status
In Commercial Distribution

Related devices

Category: Blood collection set, noninvasive

Other devices from Innovative Medical Technologies, Inc.

See all devices from Innovative Medical Technologies, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)