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Membrane Changer

by Sentec AG

Part of a family of 6 devices: see the family page

Ref MC

Membrane Changer (MC) is a Class I device made by SenTec AG, registered in EUDAMED on 12 Nov 2021 (Basic UDI-DI 764012188MCSR), active as of 22 Oct 2026.

Active European Union

CE MDR

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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number764012188MCSR Basic UDI-DI 17640121880930UDI-DIDate12 Nov 2021RegisteredStatusActive

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  • Withdrawn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/MDR Active

Specification

EUDAMED

Model / reference
MC
Primary DI / UDI-DI
17640121880930
Basic UDI-DI
764012188MCSR
Direct marketing DI
17640121880930
EMDN code
Z1203020405 Transcutaneous po2/pco2 monitors
Device class
Class I
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CH-MF-000008058
Authorised representative
Sentec GmbH DE-AR-000007618

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Other devices from SenTec AG

See all devices from SenTec AG →

Properties

Other properties (14, all answered No)