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UltraFlo-S 285

by Innovative Medical Technologies, Inc. 2 variants

UltraFlo-S 285 is a Class II device made by Innovative Medical Technologies, Inc., listed in FDA GUDID since 12 Mar 2026 (UDI-DI 10857182006330), 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 Number10857182006330 UDI-DI Date12 Mar 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  • Withdrawn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-S
Generic name
Blood collection set, invasive
Model / reference
285
Primary DI / UDI-DI
10857182006330
FDA product code
FMI
GMDN term
Blood collection set, invasive
Device class
Class II
Regulation number
880.5570
GUDID distribution status
In Commercial Distribution

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)