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Nelaton Catheter 8FG

by SBRG MedTech Pvt. Ltd. EUDAMED

Active European Union

Ref 03020508Model NELATON CATHETER

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number89061712503055W Basic UDI-DIDate25 Sep 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

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.

Specification

EUDAMED

Device Name
Nelaton Catheter
Model / Reference
NELATON CATHETER, 03020508
Primary DI / UDI-DI
08906171250942
Basic UDI-DI
89061712503055W
EMDN Code
U01010501 Nelaton catheters, self-lubricating
Device Class
Class IIa
Market of Registration
Türkiye

Manufacturer details

EUDAMED SRN
IN-MF-000038015
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from SBRG MedTech Pvt. Ltd.

See all devices from SBRG MedTech Pvt. Ltd. →

Properties

  • Sterile
  • Administering Medicine

Other properties (11)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No