Aorfix™ AAA Endovascular Stent Graft with Intelliflex™ Low Profile Delivery System
by Lombard Medical Limited 493 variants
Ref DE-12-51
Active
CE MDR
Valid until
20 Dec 2028
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number05055715AO01BU 05055715637145 | Date11 Apr 2024 | StatusActive |
Certificates
- 170781682 Active
Quality management system EU MDR
- Certifier
- DQS Medizinprodukte GmbH 0297
- Issued
- 21 Dec 2023
- Expires
- 20 Dec 2028
- 170781685 Active
Technical documentation EU MDR
- Certifier
- DQS Medizinprodukte GmbH 0297
- Issued
- 21 Dec 2023
- Expires
- 20 Dec 2028
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Aorfix™ AAA Endovascular Stent Graft with Intelliflex™ Low Profile Delivery System
- Model / Reference
- DE-12-51
- Primary DI / UDI-DI
- 05055715637145
- Basic UDI-DI
- 05055715AO01BU, B-05055715637145
- EMDN Code
- C019009 Aortic occlusion systems
- Device Class
- Class III
- EU market of registration
- Spain
Manufacturer details
- EUDAMED SRN
- GB-MF-000014515
- Authorised representative
- Medical Device Management Ltd IE-AR-000002496
Other devices from Lombard Medical Limited
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