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PINOFIT Cold Pack large

EUDAMED

Class I (EU MDR)

Ref 30973

by PINO Pharmazeutische Präparate GmbH

Identity

Trade Name
PINOFIT Cold Pack large EUDAMED
Device Name
PINOFIT Cold Pack EUDAMED
Model / Reference
30973 EUDAMED

Identifiers

Primary DI / UDI-DI
04260408932785 EUDAMED
Basic UDI-DI
426040893COLDPACKQX EUDAMED
Direct Marketing DI
04260408932785 EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

PINOFIT Cold Pack large by PINO Pharmazeutische Präparate GmbH — 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
DE-MF-000005667

Sources (1)

  • EUDAMED b42abf6f-422e-404b-b4c1-691388148b84 61 fields · synced Aug 2, 2026