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ManuXelect 1550000

by Enraf-Nonius B.V.

Ref XBnnnnnn

ManuXelect 1550000 is a Class I device made by Enraf-Nonius B.V., registered in EUDAMED on 22 May 2026 (Basic UDI-DI 871999250815500002V) and listed in FDA GUDID since 8 Jun 2023 (UDI-DI 08719992508068), active as of 23 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number871999250815500002V Basic UDI-DI 08719992508068UDI-DIDate22 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number08719992508068 UDI-DI Date8 Jun 2023ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 871999250815500002V registered 22 May 2026 Active
  • FDA GUDID UDI-DI 08719992508068 listed 8 Jun 2023 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 08719992508068
  2. Registered EUDAMED 871999250815500002V

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
ManuXelect
Generic name
Examination/treatment table, line-powered
Model / reference
XBnnnnnn EUDAMED
1550000 GUDID
Primary DI / UDI-DI
08719992508068
Basic UDI-DI
871999250815500002V
Direct marketing DI
08719992508068
FDA product code
INQ
EMDN code
Z120602 Physiotherapy equipment
GMDN term
Examination/treatment table, line-powered
Device class
Class I
Regulation number
890.3760
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / referenceEUDAMED
XBnnnnnn
GUDID
1550000

Related devices

Category: Examination/treatment table, line-powered

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Other devices filed under PHYSIOTHERAPY EQUIPMENT.

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Properties

  • Prescription use
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (21, all answered No)