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eRAD PACS 9

by Erad, Inc.

eRAD PACS 9 is a Class II device made by Erad, Inc., listed in FDA GUDID since 30 Oct 2023 (UDI-DI 00866994000255), 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 Number00866994000255 UDI-DI Date30 Oct 2023ListedStatusListed 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  • Withdrawn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
eRAD PACS
Generic name
Radiological PACS-dedicated management software
Model / reference
9
Primary DI / UDI-DI
00866994000255
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

Related devices

Category: Radiological PACS software

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Other devices filed under Radiological PACS software.

Other devices from Erad, Inc.

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Properties

  • Serial number
Other properties (14, all answered No)