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Froster Bl 180 Pro-Active F

EUDAMED

Class IIa (EU MDR)

Ref 10230

by Philipp Kirsch GmbH

Identity

Trade Name
FROSTER BL 180 PRO-ACTIVE F EUDAMED
Device Name
FROSTER BL PRO-ACTIVE EUDAMED
Model / Reference
10230 EUDAMED

Identifiers

Primary DI / UDI-DI
04260688580171 EUDAMED
Basic UDI-DI
426068858BLFROSTERPAJD EUDAMED
EMDN Code
Z121702 BLOOD AND BLOOD COMPONENTS FREEZERS 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

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

Froster Bl 180 Pro-Active F by Philipp Kirsch GmbH — 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

Manufacturer
Philipp Kirsch GmbH
EUDAMED SRN
DE-MF-000005605

Sources (1)

  • EUDAMED 0e625760-7e8e-467d-b32a-a6e90ed9758e 61 fields · synced Jun 19, 2026