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Membrane Changer

EUDAMED

Class I (EU MDR)

Ref MC

by Sentec AG

Identity

Trade Name
Membrane Changer EUDAMED
Device Name
Membrane Changer EUDAMED
Model / Reference
MC EUDAMED

Identifiers

Primary DI / UDI-DI
17640121880930 EUDAMED
Basic UDI-DI
764012188MCSR EUDAMED
Direct Marketing DI
17640121880930 EUDAMED
EMDN Code
Z1203020405 TRANSCUTANEOUS PO2/PCO2 MONITORS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Membrane Changer by SenTec AG — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Sentec AG
EUDAMED SRN
CH-MF-000008058
Authorised Representative
Sentec GmbH DE-AR-000007618

Sources (1)

  • EUDAMED dd234a87-7ed6-4429-851f-b4596d86593f 61 fields · synced Jun 19, 2026