Abs
by Lifetech Scientific (Shenzhen) Co., Ltd. China EUDAMED
Ref PS-C-10080L
EMDN P070401020103
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number69383701005000UR | Date13 Mar 2026 | StatusActive |
Coverage
- Active
- Not covered
European Union — CE/MDR Active
Certificates
- 2259149TD12 Amended
Technical documentation EU MDR
- Notified body
- Notified body 0344
- Issued
- 1 Sep 2026
- Expires
- 1 Feb 2031
- Reason
- Other
- 2259149CE01 Supplemented
Quality management system EU MDR
- Notified body
- Notified body 0344
- Issued
- 29 Aug 2026
- Expires
- 1 Aug 2027
- Reason
- Add device or group
Specification
- Device Name
- G-iliac™ Iliac Bifurcation Device, composed of G-iliac™ Iliac Bifurcation Stent Graft System and SilverFlow™ Internal Iliac Stent Graft System
- Model / Reference
- PS-C-10080L
- Primary DI / UDI-DI
- 06938370165286
- Basic UDI-DI
- 69383701005000UR
- EMDN Code
- P070401020103 Ptfe vascular endoprostheses, straight - peripheral
- Device Class
- Class III
- 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 & raw data
Show properties, registry sources and raw records
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
Sources (1)
- EUDAMED 06938370165286|69383701005000UR