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Envoke™ Catheter

by NeuroVasc Technologies, Inc. United States EUDAMED

Ref FG-005-1415Model Envoke Catheter, 017, 135 cm, Coil Regular EMDN C0104020202

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-00810029781022 Basic UDI-DIDate17 Apr 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  • Withdrawn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 · synced 25 Oct 2026

Device Name
Envoke
Model / Reference
Envoke Catheter, 017, 135 cm, Coil Regular, FG-005-1415
Primary DI / UDI-DI
00810029781022
Basic UDI-DI
B-00810029781022
EMDN Code
C0104020202 Peripheral embolisation catheters and microcatheters
Device Class
Class III
Market of Registration
Netherlands

Manufacturer details

EUDAMED SRN
US-MF-000017356
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Other devices from NeuroVasc Technologies, Inc.

See all devices from NeuroVasc Technologies, Inc. →

Properties & raw data

Show properties, registry sources and raw records
  • 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

Sources (1)

  • EUDAMED b3340064-7f9f-4e83-8910-200fa0f25d60 61 fields · synced 25 Oct 2026