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Anesthesia Kit

by Henan Tuoren Medical Device Co., Ltd 81 variants

Ref STM251Model Spinal Kit (AS-S)

Active European Union

CE MDR

Valid until

11 Nov 2030

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

2 certificates

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 Number693811933356J9 Basic UDI-DI Date8 Apr 2026RegisteredStatusActive

Certificates

2 certificates · EUDAMED

EUDAMED certificates (2)

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Anesthesia Kit
Model / Reference
Spinal Kit (AS-S), STM251
Primary DI / UDI-DI
16938119334093, 26938119334090, 06938119334096
Basic UDI-DI
693811933356J9
EMDN Code
A01030101 Spinal 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