Nexus
Ref ESN200DETS3618931Model Descending system
Active
CE MDR
Valid until
23 Jun 2031
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | NumberG70 132171 0004 | Date12 Oct 2026 | StatusActive |
Certificates
- G70 132171 0004 Active
Technical documentation EU MDR
- Certifier
- TÜV SÜD Product Service GmbH 0123
- Issued
- 12 Oct 2026
- Expires
- 23 Jun 2031
- Reason
- Add device or group
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- NEXUS® Aortic Arch Stent Graft System
- Model / Reference
- Descending system, ESN200DETS3618931
- Primary DI / UDI-DI
- 07290116282121
- Basic UDI-DI
- 729011628ESN200DEG8
- EMDN Code
- P070102010201 Dacron vascular prostheses, multifurcated (aortic arch (also collateral and multiple) and thoracic-abdominal)
- Device Class
- Class III
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- IL-MF-000014169
- Authorised representative
- MedNet EC-REP III GmbH DE-AR-000011191
Other devices from Endospan Ltd
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