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Obstetrix

by Cerner Corporation 2 variants

Ref 135650

Obstetrix (135650) is a Class I device made by Cerner Corporation, registered in EUDAMED on 30 Oct 2026 (Basic UDI-DI B-00868541000060), active as of 7 Nov 2026.

Active European Union

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-00868541000060 Basic UDI-DI 00868541000060UDI-DIDate30 Oct 2026RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Model / reference
135650
Primary DI / UDI-DI
00868541000060
Basic UDI-DI
B-00868541000060
EMDN code
Z12040182 General medicine diagnosis and monitoring instruments - software accessories
Device class
Class I
EU registration type
Legacy device (under a directive)
EU market of registration
Sweden

Manufacturer details

EUDAMED SRN
US-MF-000007215
Authorised representative
Oracle Nederland BV NL-AR-000038897

Similar devices in this category

Other devices filed under GENERAL MEDICINE DIAGNOSIS AND MONITORING INSTRUMENTS - SOFTWARE ACCESSORIES.

Other devices from Cerner Corporation

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Properties

Other properties (12, all answered No)