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Heka Cold/Hot Pack

EUDAMED

Class I (EU MDR)

Ref KW0200B-1

by Allion BV h.o.d.n. van Heek Medical

Identity

Trade Name
Heka Cold/Hot Pack EUDAMED
Device Name
Hot/Cold Pack EUDAMED
Model / Reference
KW0200B-1 EUDAMED

Identifiers

Primary DI / UDI-DI
08715886028674 EUDAMED
Basic UDI-DI
8715886HotColdPackAB EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands 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: Device sterilization/disinfection container, reusable

Heka Cold/Hot Pack by Allion BV h.o.d.n. van Heek Medical — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
NL-MF-000003490

Sources (1)

  • EUDAMED 09b6d812-aad0-4a51-91f0-cf41a7b65286 61 fields · synced Jun 18, 2026