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Xuper
EUDAMEDClass III (EU MDR)
Ref OS-III-36180-18161630Model Aortic stent graft
Identity
- Trade Name
- Xuper EUDAMED
- Device Name
- Xuper™ Open Surgery Stent Graft System EUDAMED
- Model / Reference
- Aortic stent graft EUDAMEDOS-III-36180-18161630 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06938370170990 EUDAMED
- Basic UDI-DI
- B-06938370170990 EUDAMED
- EMDN Code
- P0704020299 PERIPHERAL VASCULAR STENTS - OTHER EUDAMED
Classification
- Device Class
- Class III EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
Yes
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Xuper by Lifetech Scientific (Shenzhen) Co., Ltd. — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-06938370170990 | Class III | Active |
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Manufacturer
- Manufacturer
- Lifetech Scientific (Shenzhen) Co., Ltd.
- EUDAMED SRN
- CN-MF-000001561
- Authorised Representative
- LifeTech Scientific (Europe) B.V. NL-AR-000000804
Sources (1)
- EUDAMED 59c29073-ba99-437f-9c73-2da7c5cdf610 61 fields · synced Jun 18, 2026