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The RAMP - Click Belt

by Innovative Orthopedic Technologies IOT AG

Ref 9811021

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number3701602398110008C Basic UDI-DI 03701602300471UDI-DIDate7 May 2024RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
The RAMP
Model / Reference
9811021
Primary DI / UDI-DI
03701602300471
Basic UDI-DI
3701602398110008C
Direct Marketing DI
03701602300471
EMDN Code
Z12011299 Patient positioning instruments – other
Device Class
Class I
EU market of registration
Austria

Manufacturer details

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

From the manufacturer

Manufacturer's product page: The RAMP

Other devices from Innovative Orthopedic Technologies IOT AG

See all devices from Innovative Orthopedic Technologies IOT AG →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No