← Back to catalogue

Mesa Tipo Bobath

EUDAMED

Class I (EU MDR)

Ref F.32-B

by Ortotecsa, S.l.

Identity

Trade Name
MESA TIPO BOBATH EUDAMED
Device Name
CAMILLAS EUDAMED
Model / Reference
F.32-B EUDAMED

Identifiers

Primary DI / UDI-DI
08436602179608 EUDAMED
Basic UDI-DI
843660217CAU7 EUDAMED
Direct Marketing DI
08436602179608 EUDAMED
EMDN Code
V08050101 GENERIC USE STRETCHERS 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

Mesa Tipo Bobath 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

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 5ee33df8-ee21-4b36-9a18-81d39c526765 61 fields · synced Jun 19, 2026