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The RAMP

EUDAMED

Class I (EU MDR)

Ref 9811000

by Innovative Orthopedic Technologies IOT AG

Identity

Trade Name
The RAMP EUDAMED
Device Name
The RAMP EUDAMED
Model / Reference
9811000 EUDAMED

Identifiers

Primary DI / UDI-DI
03701602300037 EUDAMED
Basic UDI-DI
3701602398110008C EUDAMED
Direct Marketing DI
03701602300037 EUDAMED
EMDN Code
Z12011299 PATIENT POSITIONING INSTRUMENTS – OTHER 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

The RAMP by Innovative Orthopedic Technologies IOT AG — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Manufacturer's product page: The RAMP

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CH-MF-000041418
Authorised Representative
Blue Broccoli GmbH LI-AR-000000233

Sources (1)

  • EUDAMED 557b8588-ec71-4f9a-8cd8-546504edbf0d 61 fields · synced Jun 19, 2026