Skip to content

DigiView 3.8

by Digisonics Inc

DigiView 3.8 is a Class II device made by Digisonics Inc, listed in FDA GUDID since 17 Jul 2020 (UDI-DI 00857050006007), 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 Number00857050006007 UDI-DI Date17 Jul 2020ListedStatusListed 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  • Withdrawn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
DigiView
Generic name
Radiological PACS-dedicated management software
Model / reference
3.8
Primary DI / UDI-DI
00857050006007
FDA product code
LLZ
GMDN term
Radiological PACS-dedicated management software
Device class
Class II
Regulation number
892.2050
GUDID distribution status
In Commercial Distribution

Similar devices in this category

Other devices filed under Radiological PACS software.

Other devices from Digisonics Inc

See all devices from Digisonics Inc →

Properties

  • Manufacturing date
Other properties (14, all answered No)