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Instant Cold Pack

EUDAMED

Class IIa (EU MDR)

Ref KK-IC-B 220

by Koolcare Technology Co., Ltd.

Identity

Device Name
Instant Cold Pack EUDAMED
Model / Reference
KK-IC-B 220 EUDAMED

Identifiers

Primary DI / UDI-DI
06974423592203 EUDAMED
Basic UDI-DI
B-06974423592203 EUDAMED
EMDN Code
M030504 IMMOBILISATION SYSTEMS, MOULDABLE UNDER COLD AND HOT TEMPERATURES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Instant Cold Pack by Koolcare Technology Co., Ltd. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
CN-MF-000017687
Authorised Representative
Prolinx GmbH DE-AR-000005129

Sources (1)

  • EUDAMED f504c8d6-927a-45b7-b5d0-4aa511825f8f 61 fields · synced Jun 18, 2026