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Prisca 4.0

by Siemens Healthcare Diagnostics Products Ltd.

Ref 11273325Model DX_LS_LEGACY_00630414228495

Prisca 4.0 (11273325) is a device classified as IVD Annex II List B made by Siemens Healthcare Diagnostics Products Limited, registered in EUDAMED on 22 Oct 2026 (Basic UDI-DI B-00630414228495), active as of 7 Nov 2026.

Active European Union

CE IVDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-00630414228495 Basic UDI-DI 00630414228495UDI-DIDate22 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/IVDD Active

Specification

EUDAMED

Device name
DX_LS_LEGACY_00630414228495
Model / reference
DX_LS_LEGACY_00630414228495, 11273325
Primary DI / UDI-DI
00630414228495
Basic UDI-DI
B-00630414228495
EMDN code
W02079092 Various general purpose IVD instruments - IVD medical device software
Device class
Class IVD Annex II List B
EU registration type
Legacy device (under a directive)
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
GB-MF-000016339
Authorised representative
Siemens Healthcare Diagnostics Manufacturing Limited IE-AR-000006763

Similar devices in this category

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

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Properties

  • Professional testing
Other properties (12, all answered No)