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SafeID 2.0

by Vision RT Limited

SafeID 2.0 is a Class I device made by Vision RT Limited, listed in FDA GUDID since 23 Dec 2025 (UDI-DI 05056190500658), 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 Number05056190500658 UDI-DI Date23 Dec 2025ListedStatusListed 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  • Withdrawn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
SafeID
Generic name
Patient-administration information system application software
Model / reference
SafeID 2.0
Primary DI / UDI-DI
05056190500658
FDA product code
OUG
GMDN term
Patient-administration information system application software
Device class
Class I
Regulation number
880.6310
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code OUG (Medical Device Data System).

Other devices from Vision RT Limited

See all devices from Vision RT Limited →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)