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Futhrough

by Lifetech Scientific (Shenzhen) Co., Ltd. 21 variants

Ref LT-SGB-46-100-35

Expiring European Union

CE MDR

Valid until

1 Aug 2027

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

2 certificates

Certifier DEKRA Certification B.V.

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 Number2259149CE06 Date4 Sep 2026IssuedStatusExpiring expires 1 Aug 2027

Certificates

2 certificates · EUDAMED

EUDAMED certificates (2)
  • 2259149TD14 Active

    Technical documentation EU MDR

    Certifier
    DEKRA Certification B.V. 0344
    Issued
    4 Sep 2026
    Expires
    1 Sep 2031
  • 2259149CE06 Expiring Expires in 273 days

    Quality management system EU MDR

    Certifier
    DEKRA Certification B.V. 0344
    Issued
    4 Sep 2026
    Expires
    1 Aug 2027

Coverage

1 jurisdiction

NorwayIcelandSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaLiechtensteinAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyTürkiyeCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Expiring

Map note: Northern Ireland has no dot of its own.

  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Greece
  • Hungary
  • Iceland
  • Ireland
  • Italy
  • Latvia
  • Liechtenstein
  • Lithuania
  • Luxembourg
  • Malta
  • Netherlands
  • Northern Ireland
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • Sweden
  • Türkiye

Specification

EUDAMED

Device Name
FuthroughTM Stent Graft Balloon Catheter
Model / Reference
LT-SGB-46-100-35
Primary DI / UDI-DI
06938370138990
Basic UDI-DI
69383701009500WE
EMDN Code
C010402020102 Stent positioning vascular balloon dilatation catheters
Device Class
Class III
EU market of registration
Austria

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

  • Sterile

Other properties (12)

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