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Anesthesia Needle

by Henan Tuoren Medical Device Co., Ltd 10 variants

Ref EAN19Model AN-E (Epidural needle)

Active European Union

CE MDR

Valid until

11 Nov 2030

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier Intertek Medical Notified Body AB

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/MDR Number693811933360HY Basic UDI-DI Date22 Apr 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Anesthesia Needle
Model / Reference
AN-E (Epidural needle), EAN19
Primary DI / UDI-DI
06941617120566, 16941617120563
Basic UDI-DI
693811933360HY
EMDN Code
A01030102 Epidural anaesthesia needles and kits
Device Class
Class III
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
CN-MF-000013924
Authorised representative
MedNet EC-REP C III GmbH DE-AR-000011196

Other devices from Henan Tuoren Medical Device Co., Ltd.

See all devices from Henan Tuoren Medical Device Co., 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