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Neo+

by Daytot XI EUDAMED

Ref 208-600

EMDN V080302

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5065012224208QL Basic UDI-DIDate21 Apr 2023RegisteredStatusWithdrawn

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Withdrawn
  • Not covered

European Union — CE/MDR Withdrawn

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
Neo+
Model / Reference
208-600
Primary DI / UDI-DI
05065012224122
Basic UDI-DI
5065012224208QL
Direct Marketing DI
05065012224122
EMDN Code
V080302 Patient positioning medical cushions
Device Class
Class I
Market of Registration
Northern Ireland

Manufacturer details

EUDAMED SRN
XI-MF-000025474

Other devices from Daytot

  • Joey

    Class I

Properties & raw data

Show properties, registry sources and raw records
Other properties (13)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED d4dae606-8571-4bf5-b14f-bbf35ba58796 61 fields · synced 22 Oct 2026