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RamSoft 202408

by Ramsoft Inc

RamSoft 202408 (OAIIV202408) is a Class II device made by Ramsoft Inc, listed in FDA GUDID since 6 Sep 2024 (UDI-DI B359OAIIV2024081), 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 NumberB359OAIIV2024081 UDI-DI Date6 Sep 2024ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
RamSoft
Generic name
Radiology information system application software
Model / Ref / Catalog
202408, OAIIV202408
Primary DI / UDI-DI
B359OAIIV2024081
FDA product code
LLZ
GMDN term
Radiology information system application software
Device class
Class II
Regulation number
892.2050
GUDID distribution status
In Commercial Distribution

Related devices

Category: Radiological PACS softwareRadiology picture archiving and communication system workstationRadiology information system application software

Other devices from Ramsoft Inc

See all devices from Ramsoft Inc →

Properties

  • Lot / batch number
  • Manufacturing date
Other properties (13, all answered No)