Abdominal aorta endovascular stent-graft
United Kingdom·General Medical Device·Cordis Cashel·Registered Nov 26, 2024- Device ID
- 160521
- MHRA Reference Number
- 160521
- Date Registered
- Nov 26, 2024
- Last Updated
- Nov 10, 2023
- Device Type
- General Medical Device
- Devices
- Abdominal aorta endovascular stent-graft
- Type
- Class III
- Name
- Cordis Cashel
- Address
- Cahir Road Cashel, Co. Tipperary, Ireland
- Created Date
- Nov 14, 2022
- Relationship Type
- UK Responsible Person
- Address
- Suite 402, Chadwick House Birchwood Park Warrington, England, United KingdomPostcode: WA3 6AE
Devices with a matching generic name or device type registered with MHRA
Additional devices registered by the same manufacturer
Additional devices represented by Cordis Medical UK Limited in the UK
Abdominal aorta endovascular stent-graft is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 160521. The device is manufactured by Cordis Cashel from Ireland, classified as General Medical Device. The authorized representative in the UK is Cordis Medical UK Limited.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.