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Cryopush

EUDAMED

Class I (EU MDR)

Ref KRP/LFQ-H20-MModel KRP/LFQ-(CO,A20,B20,C20,E20,F20,G20,H20,I20,J20)-M

by Chengdu Cryo-Push Medical Technology Co., Ltd

Identity

Trade Name
CRYOPUSH EUDAMED
Device Name
Cold Therapy System EUDAMED
Model / Reference
KRP/LFQ-(CO,A20,B20,C20,E20,F20,G20,H20,I20,J20)-M EUDAMED
KRP/LFQ-H20-M EUDAMED

Identifiers

Primary DI / UDI-DI
06973641883582 EUDAMED
Basic UDI-DI
697364188LFQVA EUDAMED
EMDN Code
M9001 CRYOTHERAPY AND THERMOTHERAPY DEVICES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Greece 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

Category: Hot/cold therapy pack, reusable

Cryopush by Chengdu Cryo-push Medical Technology Co., Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Hot/cold therapy pack, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

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

Sources (1)

  • EUDAMED 86fb9a3a-82d4-4b81-831a-52ee381fb9f5 61 fields · synced May 23, 2026