← Back to catalogue

Cold Wrap

EUDAMED

Class I (EU MDR)

Ref KRP/FD-A3-MModel KRP/FD-(A3,B3,C3,D3,E3,F3,G3,H3,I3,J3,K3,L3)-M

by Chengdu Cryo-Push Medical Technology Co., Ltd

Identity

Device Name
Cold Wrap EUDAMED
Model / Reference
KRP/FD-(A3,B3,C3,D3,E3,F3,G3,H3,I3,J3,K3,L3)-M EUDAMED
KRP/FD-A3-M EUDAMED

Identifiers

Primary DI / UDI-DI
06973641880055 EUDAMED
Basic UDI-DI
697364188FD1S8 EUDAMED
EMDN Code
M9001 CRYOTHERAPY AND THERMOTHERAPY DEVICES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France 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

Cold Wrap 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (1)

  • EUDAMED 978cb7e2-8de6-47e9-a9a3-9d4f34c4e68f 61 fields · synced Jul 29, 2026