Skip to content

Futhrough

by Lifetech Scientific (Shenzhen) Co., Ltd. China EUDAMED

Ref LT-FIS-17G6F035

EMDN A01010302

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-06938370136163 Basic UDI-DIDate15 Dec 2022RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Futhrough™ Endovascular needle system
Model / Reference
LT-FIS-17G6F035
Primary DI / UDI-DI
06938370136163
Basic UDI-DI
B-06938370136163
EMDN Code
A01010302 Needles and kits for implantable systems (port), w/o safety systems
Device Class
Class III
Market of Registration
Greece

Manufacturer details

EUDAMED SRN
CN-MF-000001561
Authorised representative
LifeTech Scientific (Europe) B.V. NL-AR-000000804

Other devices from Lifetech Scientific (Shenzhen) Co., Ltd.

See all devices from Lifetech Scientific (Shenzhen) Co., Ltd. →

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 e5f7ec7b-794d-4f4a-ada0-3f5450f8b2fe 61 fields · synced 24 Oct 2026