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Intracuff Pressure Monitor

by Rmist(Tianjin) Medical Device Co., Ltd. 12 variants

Model IPM1 IPM2 IPM3 IPM4

Active European Union

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697307763IPMU7 Basic UDI-DI 06976651242493UDI-DIDate11 Dec 2025RegisteredStatusActive

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  • Withdrawn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

Device Name
Intracuff Pressure Monitor
Model / Reference
IPM1 IPM2 IPM3 IPM4
Primary DI / UDI-DI
06976651242493
Basic UDI-DI
697307763IPMU7
EMDN Code
R018099 Intubation devices - accessories not included in other classes - other
Device Class
Class I
EU market of registration
Cyprus

Manufacturer details

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

Other devices from Rmist(Tianjin) Medical Device Co., Ltd.

See all devices from Rmist(Tianjin) Medical Device Co., Ltd. →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No