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Dr. Max Instant Cold Pack

EUDAMED

Class IIa (EU MDR)

Ref KK-IN-200g

by Koolcare Technology Co., Ltd.

Identity

Trade Name
Dr. Max Instant Cold Pack EUDAMED
Device Name
Instant Cold Pack EUDAMED
Model / Reference
KK-IN-200g EUDAMED

Identifiers

Primary DI / UDI-DI
08595566421380 EUDAMED
Basic UDI-DI
697442359ICBS3 EUDAMED
EMDN Code
Z120602 PHYSIOTHERAPY EQUIPMENT EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Czechia 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

Dr. Max Instant Cold Pack by Koolcare Technology Co., Ltd. — Class IIa — 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-000017687
Authorised Representative
Prolinx GmbH DE-AR-000005129

Sources (1)

  • EUDAMED 9ce8f4d3-a201-4b68-a8ce-6724791b3ea2 61 fields · synced Jun 19, 2026