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Pronosupinador

EUDAMED

Class I (EU MDR)

Ref F.42/47

by Ortotecsa, S.l.

Identity

Trade Name
PRONOSUPINADOR EUDAMED
Device Name
ROTACIÓN EUDAMED
Model / Reference
F.42/47 EUDAMED

Identifiers

Primary DI / UDI-DI
08436602171732 EUDAMED
Basic UDI-DI
843660217ROWG EUDAMED
Direct Marketing DI
08436602171732 EUDAMED
EMDN Code
Y0504 ARMS, TORSO AND LEGS RE-EDUCATION DEVICES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Spain 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

Pronosupinador by Ortotecsa, S.l. — 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

Manufacturer
Ortotecsa, S.l.
EUDAMED SRN
ES-MF-000004786

Sources (1)

  • EUDAMED 7b0e71e9-9441-4a1d-85dd-5436de28ed0e 61 fields · synced Aug 1, 2026