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EOS Portal 2.14

by Eos Imaging

EOS Portal 2.14 is a Class I device made by Eos Imaging, listed in FDA GUDID since 10 Jul 2023 (UDI-DI 03663999000191), not in commercial distribution (GUDID) as of 12 Nov 2026.

Listed FDA GUDID listing, not in commercial distribution

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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number03663999000191 UDI-DI Date10 Jul 2023ListedStatusListed GUDID: not 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  • Withdrawn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
EOS Portal
Generic name
Multidisciplinary medical image management software
Model / reference
2.14
Primary DI / UDI-DI
03663999000191
FDA product code
LMD
GMDN term
Multidisciplinary medical image management software
Device class
Class I
Regulation number
892.2020
GUDID distribution status
Not in Commercial Distribution

Similar devices

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

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See all devices from Eos Imaging →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)