Skip to content

EchoGo Workstream 1.0

by Ultromics, Ltd.

EchoGo Workstream 1.0 is a Class I device made by Ultromics, Ltd., listed in FDA GUDID since 14 Jan 2026 (UDI-DI 05060634690072), 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 Number05060634690072 UDI-DI Date14 Jan 2026ListedStatusListed 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  • Withdrawn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
EchoGo
Generic name
Radiology DICOM image processing application software
Model / reference
Workstream 1.0
Primary DI / UDI-DI
05060634690072
FDA product code
LMD
GMDN term
Radiology DICOM image processing application software
Device class
Class I
Regulation number
892.2020
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code LMD (System, Digital Image Communications, Radiological).

Other devices from Ultromics, Ltd.

  • EchoGo Core

    Class II
  • EchoGo Heart Failure 2.0

    Class II
  • EchoGo Core 2.0

    Class II
  • EchoGo Amyloidosis 1.0

    Class II

See all devices from Ultromics, Ltd. →

Properties

  • Prescription use
  • Premarket exempt
Other properties (13, all answered No)