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Xuper

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

Ref OS-I-28120-1230Model Aortic stent graft EMDN P0704020299

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-06938370110194 Basic UDI-DIDate8 Mar 2024RegisteredStatusActive

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  • Withdrawn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 24 Oct 2026

Device Name
Xuper™ Open Surgery Stent Graft System
Model / Reference
Aortic stent graft, OS-I-28120-1230
Primary DI / UDI-DI
06938370110194
Basic UDI-DI
B-06938370110194
EMDN Code
P0704020299 Peripheral vascular stents - other
Device Class
Class III
Market of Registration
Germany

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
  • Implantable
Other properties (9)
  • 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 6cc87329-3a41-46a2-9a47-cca1151d264c 61 fields · synced 24 Oct 2026