← Back to catalogue

Bendiboard

EUDAMED

Class I (EU MDR)

Ref BB003Model BB001

by Conlett Technology Inc

Identity

Trade Name
Bendiboard EUDAMED
Device Name
Bendiboard EUDAMED
Model / Reference
BB001 EUDAMED
BB003 EUDAMED

Identifiers

Primary DI / UDI-DI
06973596010545 EUDAMED
Basic UDI-DI
697359601BendiboardY7 EUDAMED
Direct Marketing DI
06973596010545 EUDAMED
EMDN Code
Y061299 LOWER EXTREMITY ORTHOSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Belgium EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Bendiboard by Conlett Technology Inc — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (1)

  • EUDAMED 68094100-b35d-4a4a-ac39-39110d044ab9 61 fields · synced Jun 18, 2026