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Epidural needle

by Zhejiang Runqiang Medical Instruments Co., Ltd EUDAMED

Active European Union

Ref NRF0318035Model AN-E

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697374067004LM Basic UDI-DIDate10 Jul 2025RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)

Specification

EUDAMED

Device Name
Disposable Anaesthesia Needle and Anaesthesia Kit
Model / Reference
AN-E, NRF0318035
Primary DI / UDI-DI
06973740678898
Basic UDI-DI
697374067004LM
Direct Marketing DI
06973740678898
EMDN Code
A01030102 Epidural anaesthesia needles and kits
Device Class
Class III
Market of Registration
France

Manufacturer details

EUDAMED SRN
CN-MF-000005693
Authorised representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Other devices from Zhejiang Runqiang Medical Instruments Co., Ltd

See all devices from Zhejiang Runqiang Medical Instruments Co., Ltd →

Properties

  • Sterile
  • CMR Substance

Other properties (11)

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