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Intracuff Pressure Monitor

EUDAMED

Class I (EU MDR)

Ref NoneModel IPM1 IPM2 IPM3 IPM4

by Rmist(Tianjin) Medical Device Co., Ltd.

Identity

Device Name
Intracuff Pressure Monitor EUDAMED
Model / Reference
IPM1 IPM2 IPM3 IPM4 EUDAMED
None EUDAMED

Identifiers

Primary DI / UDI-DI
26976651243852 EUDAMED
Basic UDI-DI
697307763IPMU7 EUDAMED
EMDN Code
R018099 INTUBATION DEVICES - ACCESSORIES NOT INCLUDED IN OTHER CLASSES - OTHER 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

Intracuff Pressure Monitor by Rmist(Tianjin) Medical Device Co., Ltd. — 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

EUDAMED SRN
CN-MF-000010408
Authorised Representative
Caretechion GmbH DE-AR-000005946

Sources (1)

  • EUDAMED 2779f649-10a8-49cc-bfaa-2ed55a217b58 61 fields · synced Jun 19, 2026