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Cryopush

by Chengdu Cryo-Push Medical Technology Co., Ltd 12 variants

Ref KRP/QN-H2Model KRP/QN-[A2,B2(M),B2(L),C2,D2,E2,F2,G2,H2,K2,N2]

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697364188QN2UX Basic UDI-DI 06973641889348UDI-DIDate24 Aug 2026RegisteredStatusActive

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  • Withdrawn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
Cold Compression Wrap 2.0
Model / Reference
KRP/QN-[A2, B2(M), B2(L), C2, D2, E2, F2, G2, H2, K2, N2], KRP/QN-H2
Primary DI / UDI-DI
06973641889348
Basic UDI-DI
697364188QN2UX
EMDN Code
M9001 Cryotherapy and thermotherapy devices
Device Class
Class I
EU market of registration
Slovakia

Manufacturer details

EUDAMED SRN
CN-MF-000019527
Authorised representative
MedNet EC-REP GmbH DE-AR-000000002

Other devices from Chengdu Cryo-push Medical Technology Co., Ltd.

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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