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PINOFIT Kombi-Seilzugapparat Standard

EUDAMED

Class I (EU MDR)

Ref 6012008

by PINO Pharmazeutische Präparate GmbH

Identity

Trade Name
PINOFIT Kombi-Seilzugapparat Standard EUDAMED
Device Name
PINOFIT Rope pulley EUDAMED
Model / Reference
6012008 EUDAMED

Identifiers

Primary DI / UDI-DI
04260730028132 EUDAMED
Basic UDI-DI
426040893SEILZUG31KL EUDAMED
Direct Marketing DI
04260730028132 EUDAMED
EMDN Code
Z120602 PHYSIOTHERAPY EQUIPMENT 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

PINOFIT Kombi-Seilzugapparat Standard by PINO Pharmazeutische Präparate GmbH — Class I — 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
DE-MF-000005667

Sources (1)

  • EUDAMED d478f171-4e47-4044-b395-fa70dba94663 61 fields · synced Jul 14, 2026