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Ultrasound-visible Puncture Needles for Nerve Block

by Hunan ShineArk Medical Technology Co., Ltd. 48 variants

Ref AN-N 22G(0.7×80)Model AN-N

Active European Union

CE MDR

Valid until

4 Nov 2030

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier Eurofins Product Testing Italy S.r.l.

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberEPT 0477.MDR.25/5975 Date5 Nov 2025IssuedStatusActive expires 4 Nov 2030

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • EPT 0477.MDR.25/5975 Active

    Quality management system EU MDR

    Certifier
    Eurofins Product Testing Italy S.r.l. 0477
    Issued
    5 Nov 2025
    Expires
    4 Nov 2030

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
AN-N, AN-N 22G(0.7×80)
Primary DI / UDI-DI
06976934381925
Basic UDI-DI
697693438AN-N52MX
Direct Marketing DI
06976934381925
EMDN Code
A010302 Plexus block needles and kits
Device Class
Class IIa
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
CN-MF-000045256
Authorised representative
HUMISS TRADING S. L. ES-AR-000040177

Other devices from Hunan ShineArk Medical Technology Co., Ltd.

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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