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ultrasonic transducer E741

by Edan Instruments, Inc.

ultrasonic transducer E741 is a Class II device made by Edan Instruments, Inc., listed in FDA GUDID since 1 Sep 2016 (UDI-DI 06944413806146), 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 Number06944413806146 UDI-DI Date1 Sep 2016ListedStatusListed 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  • Withdrawn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
ultrasonic transducer
Generic name
Extracorporeal ultrasound imaging transducer, hand-held
Model / reference
E741
Primary DI / UDI-DI
06944413806146
FDA product code
ITX
GMDN term
Extracorporeal ultrasound imaging transducer, hand-held
Device class
Class II
Regulation number
892.1570
GUDID distribution status
In Commercial Distribution

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Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)