Skip to content

BoBo Pro 2.0

by Bo&Bo Ltd

Ref 8600086890162

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 Number08600086890PROMOTION6Y Basic UDI-DI 08600086890162UDI-DIDate30 Aug 2026RegisteredStatusActive

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  • Withdrawn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
BoBo Pro 2.0 and BoBo Motion 2.0
Model / Reference
8600086890162
Primary DI / UDI-DI
08600086890162
Basic UDI-DI
08600086890PROMOTION6Y
EMDN Code
Z12062402 Positional biofeedback systems
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
IL-MF-000058090
Authorised representative
Obelis s.a. BE-AR-000000106

From the manufacturer

Manufacturer's product page: BoBo Pro

Other devices from Bo&Bo Ltd

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