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PINOFIT Rumpfheber

EUDAMED

Class I (EU MDR)

Ref 48118

by PINO Pharmazeutische Präparate GmbH

Identity

Trade Name
PINOFIT Rumpfheber EUDAMED
Device Name
PINOFIT Rumpfheber EUDAMED
Model / Reference
48118 EUDAMED

Identifiers

Primary DI / UDI-DI
04260730021034 EUDAMED
Basic UDI-DI
426040893RUMPFHEBER29BL EUDAMED
Direct Marketing DI
04260730021034 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 Rumpfheber 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 f05ca853-733e-4f55-b614-6a0c05727467 61 fields · synced Jun 18, 2026