YuranosTM Aorto-Uni-Iliac Stent Graft System
by Lifetech Scientific (Shenzhen) Co., Ltd.
Ref AUI-2010-50-100
Expiring
CE MDR
Valid until
1 Aug 2027
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number2259149TD13 | Date1 Sep 2026 | StatusActive |
Certificates
- 2259149TD13 Active
Technical documentation EU MDR
- Certifier
- DEKRA Certification B.V. 0344
- Issued
- 1 Sep 2026
- Expires
- 1 Aug 2031
- Reason
- Other
- 2259149CE01 Expiring
Quality management system EU MDR
- Certifier
- DEKRA Certification B.V. 0344
- Issued
- 29 Aug 2026
- Expires
- 1 Aug 2027
- Reason
- Add device or group
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Expiring
Specification
- Device Name
- Yuranos Abdominal Aortic Stent Graft System
- Model / Reference
- AUI-2010-50-100
- Primary DI / UDI-DI
- 06938370194194
- Basic UDI-DI
- 69383701004900VX
- EMDN Code
- P070401010101 Dacron vascular endoprostheses, straight - abdominal
- Device Class
- Class III
- EU market of registration
- Greece
Manufacturer details
- EUDAMED SRN
- CN-MF-000001561
- Authorised representative
- LifeTech Scientific (Europe) B.V. NL-AR-000000804
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Properties
Other properties (11)
- 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