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Medinel

by Global Medikit Limited 20 variants

Ref 5012125Model Nelaton catheter

Medinel (5012125) is a Class IIa device made by Global Medikit Limited, registered in EUDAMED on 28 Oct 2026 (Basic UDI-DI 8903545GMLNEC011FL), active as of 7 Nov 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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8903545GMLNEC011FL Basic UDI-DI 08903545081843UDI-DIDate28 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
Nelaton catheter, 5012125
Primary DI / UDI-DI
08903545081843
Basic UDI-DI
8903545GMLNEC011FL
EMDN code
U01010502 Nelaton catheters, non self-lubricating
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
IN-MF-000013635
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from Global Medikit Limited

See all devices from Global Medikit Limited →

Properties

  • Supplied sterile
Other properties (13, all answered No)