Skip to content

Neo-Board

by Conlett Technology Inc 3 variants

Ref NB001, NB003

Neo-Board (NB001) is a Class I device made by Conlett Technology Inc, registered in EUDAMED on 23 Oct 2024 (Basic UDI-DI 697359601Neo-Board46), 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 Number697359601Neo-Board46 Basic UDI-DI Date23 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  • Withdrawn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
NB001, NB003
Primary DI / UDI-DI
06973596010569, 06973596010583
Basic UDI-DI
697359601Neo-Board46
Direct marketing DI
06973596010569
06973596010583
EMDN code
Y060699 Orthoses, upper extremity - 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 ORTHOSES, UPPER EXTREMITY - OTHER.

Other devices from Conlett Technology Inc

See all devices from Conlett Technology Inc →

Properties

Other properties (14, all answered No)