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Neo-Board

EUDAMED

Class I (EU MDR)

Ref NB001Model NB001 Ref NB003

by Conlett Technology Inc

Identity

Trade Name
Neo-Board EUDAMED
Device Name
Neo-Board EUDAMED
Model / Reference
NB001 EUDAMED
NB003 EUDAMED

Identifiers

Primary DI / UDI-DI
06973596010569 EUDAMED
06973596010583 EUDAMED
Basic UDI-DI
697359601Neo-Board46 EUDAMED
Direct Marketing DI
06973596010569 EUDAMED
06973596010583 EUDAMED
EMDN Code
Y060699 ORTHOSES, UPPER EXTREMITY - 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

Neo-Board 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

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Manufacturer

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

Sources (2)

  • EUDAMED 157f1a02-9889-4744-893d-c96a73b14a47 61 fields · synced Jul 25, 2026
  • EUDAMED 23e2ac96-e636-4347-aaa4-1bb4278e021e 61 fields · synced May 18, 2026