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Nokor

by Becton, Dickinson and Company United States EUDAMED

Ref 300780

EMDN A019001

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number038290ZHPVKFEGN2 Basic UDI-DIDate31 Jul 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 25 Oct 2026

Device Name
BD Nokor™ Admix Needle
Model / Reference
300780
Primary DI / UDI-DI
00382903007806
Basic UDI-DI
038290ZHPVKFEGN2
EMDN Code
A019001 Blunt needles
Device Class
Class I
Market of Registration
Poland

Manufacturer details

EUDAMED SRN
US-MF-000019182
Authorised representative
Becton Dickinson Ireland Limited IE-AR-000007610

Other devices from Becton, Dickinson and Company

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Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • CMR Substance
  • Administering Medicine
Other properties (10)
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 00382903007806|038290ZHPVKFEGN2 61 fields · synced 25 Oct 2026