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VivaSight-Max SA00014

by E.T. View Ltd

VivaSight-Max SA00014 is a Class II device made by E.T. View Ltd, listed in FDA GUDID since 25 Sep 2016 (UDI-DI 07290013745293), 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 Number07290013745293 UDI-DI Date25 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  • Withdrawn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
VivaSight-Max
Generic name
Image display unit, colour
Model / Ref / Catalog
SA00014
Primary DI / UDI-DI
07290013745293
FDA product code
MHX
GMDN term
Image display unit, colour
Device class
Class II
Regulation number
870.1025
GUDID distribution status
In Commercial Distribution

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Properties

  • Supplied sterile
  • Prescription use
  • Serial number
Other properties (12, all answered No)