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Ust-9132I

by Fujifilm Corporation

Ust-9132I is a Class II device made by Fujifilm Corporation, listed in FDA GUDID since 17 Jul 2021 (UDI-DI 04573596213384), registry data as of 19 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 19 Oct 2026.

Regulatory status

as of registry sync 19 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04573596213384 UDI-DI Date17 Jul 2021ListedStatusListed 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  • Withdrawn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

Generic name
Surgical ultrasound imaging transducer
Model / reference
UST-9132I
Primary DI / UDI-DI
04573596213384
FDA product code
IYO, IYN, ITX
GMDN term
Surgical ultrasound imaging transducer
Device class
Class II
Regulation number
892.1560, 892.1550, 892.1570
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical ultrasound imaging transducer

Similar devices in this category

Other devices filed under Surgical ultrasound imaging transducer.

Other devices from Fujifilm Corporation

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Properties

  • Sterilise before use
  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)