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Bendiboard

by Conlett Technology Inc 3 variants

Ref BB003Model BB001

Bendiboard (BB003) is a Class I device made by Conlett Technology Inc, registered in EUDAMED on 25 Oct 2024 (Basic UDI-DI 697359601BendiboardY7), active as of 23 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

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

Source EUDAMED, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697359601BendiboardY7 Basic UDI-DI 06973596010545UDI-DIDate25 Oct 2024RegisteredStatusActive

Official records

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  • Withdrawn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

Model / reference
BB001, BB003
Primary DI / UDI-DI
06973596010545
Basic UDI-DI
697359601BendiboardY7
Direct marketing DI
06973596010545
EMDN code
Y061299 Lower extremity orthoses - other
Device class
Class I
System or procedure pack
System which is a device in itself
EU registration type
Standard device
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
CN-MF-000002101
Authorised representative
Lotus NL B.V. NL-AR-000000121

Similar devices in this category

Other devices filed under LOWER EXTREMITY ORTHOSES - OTHER.

Other devices from Conlett Technology Inc

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Properties

Other properties (14, all answered No)