Skip to content

Sanguin Aurora 2.0

by Biomedical Data Solutions Limited

Sanguin Aurora 2.0 is a Class II device made by Biomedical Data Solutions Limited, listed in FDA GUDID since 23 Oct 2018 (UDI-DI 05060496770035), 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 Number05060496770035 UDI-DI Date23 Oct 2018ListedStatusListed 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  • Withdrawn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
Sanguin Aurora
Generic name
Blood bank information system application software
Model / reference
2.0
Primary DI / UDI-DI
05060496770035
FDA product code
MMH
GMDN term
Blood bank information system application software
Device class
Class II
Regulation number
864.9165
GUDID distribution status
In Commercial Distribution

Related devices

Category: Blood bank information system application software

Other devices from Biomedical Data Solutions Limited

See all devices from Biomedical Data Solutions Limited →

Properties

Other properties (15, all answered No)