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Veress Needle

by VHMED (Nantong) Co., Ltd. EUDAMED

Active European Union

Ref AT002, AT003, AT001

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-06971254920021 Basic UDI-DIDate31 Jan 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED

Model / Reference
AT002, AT003, AT001
Primary DI / UDI-DI
06971254920021, 06971254920038, 06971254920014
Basic UDI-DI
B-06971254920021, B-06971254920038, B-06971254920014
EMDN Code
K0104 Veress needles
Device Class
Class IIa
Market of Registration
Poland

Manufacturer details

EUDAMED SRN
CN-MF-000016558
Authorised representative
Very Heal Ltd. XI-AR-000037579

Other devices from VHMED (Nantong) Co., Ltd.

See all devices from VHMED (Nantong) Co., Ltd. →

Properties

  • Sterile

Other properties (10)

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