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TOPRO Olympos ATR

by Topro Industri AS 5 variants

Ref 122500Model TOPRO Olympos ATR

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 Number705432OLY814334 Basic UDI-DIDate30 Aug 2022RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No notified-body 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  • Withdrawn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
TOPRO Olympos ATR
Model / Reference
TOPRO Olympos ATR, 122500
Primary DI / UDI-DI
07054321225003
Basic UDI-DI
705432OLY814334
EMDN Code
Y120609 Walking frames with chair, 4 wheels
Device Class
Class I
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
NO-MF-000003447

From the manufacturer

Manufacturer's product page: TOPRO Olympos ATR Outdoor Rollator

Other devices from Topro Industri AS

See all devices from Topro Industri AS →

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