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Procleix NAT Manager 1.2

by Biomedical Data Solutions Limited

Ref 741722Model V1

Procleix NAT Manager 1.2 is a device classified as Class A in the EU and Class II in the US made by Biomedical Data Solutions Limited, registered in EUDAMED on 15 Jun 2026 (Basic UDI-DI 5060496770011Y2), listed under FDA premarket submission BK160125 and listed in FDA GUDID since 2 Oct 2018 (UDI-DI 05060496770011), active as of 24 Oct 2026.

Active European Union and United States. Also listed in GUDID (US).

CE IVDR 510(k)

Valid until

No date given

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None found

in data synced 24 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) BK160125

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR EUDAMED Number5060496770011Y2 Basic UDI-DI 05060496770011UDI-DIDate15 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number05060496770011 UDI-DI Date2 Oct 2018ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k) GUDID from GUDID NumberBK160125 Date—StatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI 5060496770011Y2 registered 15 Jun 2026 Active
  • FDA premarket submission BK160125 Active
  • FDA GUDID UDI-DI 05060496770011 listed 2 Oct 2018 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 05060496770011
  2. Registered EUDAMED 5060496770011Y2

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/IVDR Active
  • United States FDA 510(k) Active

Specification

EUDAMED · GUDID

Trade name
NAT Manager EUDAMED
Procleix NAT Manager GUDID
Generic name
Blood bank information system application software
Model / reference
V1 EUDAMED
741722 EUDAMED
1.2 GUDID
Primary DI / UDI-DI
05060496770011
Basic UDI-DI
5060496770011Y2
Direct marketing DI
05060496770011
FDA product code
PQQ
EMDN code
W02079082 Various general purpose IVD instruments - software accessories
GMDN term
Blood bank information system application software
Device class
Class A EUDAMED
Class II GUDID
Regulation number
862.2570
Special device type
Software
EU registration type
Standard device
EU market of registration
France
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
V1
741722
GUDID
1.2
Device classEUDAMED
Class A
GUDID
Class II

Device class is stated on each registry's own scale: Class A in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Blood bank information system application software

Similar devices in this category

Other devices filed under VARIOUS GENERAL PURPOSE IVD INSTRUMENTS - SOFTWARE ACCESSORIES.

Other devices from Biomedical Data Solutions Limited

See all devices from Biomedical Data Solutions Limited →

Properties

  • Professional testing
  • Prescription use
Other properties (24, all answered No)