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Bendiboard

by Conlett Technology Inc 3 variants

Ref BB002, BBS002Model BB001, Bendiboard with Straps

Bendiboard (BB002) is a Class I device made by Conlett Technology Inc, registered in EUDAMED on 25 Oct 2024 (Basic UDI-DI 697359601BendiboardY7), active as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697359601BendiboardY7 Basic UDI-DI Date25 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  • Withdrawn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

Trade name
Bendiboard
Bendiboard with Straps Medium
Device name
Bendiboard with Straps small
Model / reference
BB001, BB002, Bendiboard with Straps, BBS002
Primary DI / UDI-DI
06973596010538, 06973596011467
Basic UDI-DI
697359601BendiboardY7, 697359601BBSTA
Direct marketing DI
06973596010538
06973596011467
EMDN code
Y061299, M03050299
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
Poland

Manufacturer details

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

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Properties

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