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ULTRAMED NELATON CATHETER (TYPE : FEMALE ) Size 22 FG

by Ultra For Medical Products (Ultramed) U.M.I.C (S.A.E)

Ref 3002-22Model ULTRAMED NELATON CATHETER, ULTRAMED NELATON CATHETER ( TYPE : FEMALE ) Size 22 FG

Active European Union

CE MDR CE MDD

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD Number622300425NEC3001P9 Basic UDI-DI 06223004251849UDI-DIDate14 Mar 2026RegisteredStatusActive
European UnionCE/MDR Number622300425NEC3001P9 Basic UDI-DI 06223004251849UDI-DIDate14 Mar 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD, CE/MDR Active

Specification

EUDAMED

Device Name
Ultramed Nelaton Catheter
Ultramed Nelaton Catheter ( Type : Female )
Model / Reference
ULTRAMED NELATON CATHETER, 3002-22, ULTRAMED NELATON CATHETER ( TYPE : FEMALE ) Size 22 FG
Primary DI / UDI-DI
06223004251849
Basic UDI-DI
622300425NEC3001P9, B-06223004251849
EMDN Code
U01010502 Nelaton catheters, non self-lubricating
Device Class
Class IIa
EU market of registration
Bulgaria

Manufacturer details

EUDAMED SRN
EG-MF-000038562
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from Ultra For Medical Products (Ultramed) U.M.I.C (S.A.E)

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Properties

  • Sterile

Other properties (12)

  • 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