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E-St 60132

by Avante

E-St 60132 is a Class II device made by Avante, listed in FDA GUDID since 23 Sep 2016 (UDI-DI 00815871020367), 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 Number00815871020367 UDI-DI Date23 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  • Withdrawn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
E-St
Generic name
General-purpose ultrasound imaging system
Model / reference
60132
Primary DI / UDI-DI
00815871020367
FDA product code
HEP, KNG
GMDN term
General-purpose ultrasound imaging system
Device class
Class II
Regulation number
884.2660
GUDID distribution status
In Commercial Distribution

Related devices

Category: General-purpose ultrasound imaging system

Other devices from Avante

See all devices from Avante →

Properties

  • Serial number
  • Manufacturing date
Other properties (13, all answered No)