← Back to catalogue

Plano Estimulador Basculante

EUDAMED

Class I (EU MDR)

Ref F.15-N

by Ortotecsa, S.l.

Identity

Trade Name
PLANO ESTIMULADOR BASCULANTE EUDAMED
Device Name
ESTIMULACIÓN VESTIBULAR Y EQUILIBRIO EUDAMED
Model / Reference
F.15-N EUDAMED

Identifiers

Primary DI / UDI-DI
08436602170759 EUDAMED
Basic UDI-DI
843660217EVVP EUDAMED
Direct Marketing DI
08436602170759 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

Category: Rubber dam, Hevea-latex

Plano Estimulador Basculante by Ortotecsa, S.l. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Rubber dam, Hevea-latex.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (1)

  • EUDAMED 7456ea4c-b768-42e6-b4e4-0cb4016cb6f4 61 fields · synced Jun 19, 2026