Cardiac/peripheral vascular guidewire, single-use
United Kingdom·Active implantable device (Directive 90/385/EEC only)·Brivant Limited T/A Lake Region Medical·Registered May 5, 2021- Device ID
- 79494
- Date Registered
- May 5, 2021
- Last Updated
- Dec 22, 2022
- Device Type
- Active implantable device (Directive 90/385/EEC only)
- Devices
- Cardiac/peripheral vascular guidewire, single-use
- Type
- Active implantable Medical device
- Address
- Parkmore West Business Park Galway, Ireland
- Created Date
- May 5, 2021
- Relationship Type
- UK Responsible Person
- Address
- Compass House, Vision Park Histon c/o Cr360 – UL International Cambridge, England, United KingdomPostcode: CB24 9BZ
Devices with a matching generic name or device type registered with MHRA
Additional devices registered by the same manufacturer
Additional devices represented by Emergo Consulting (UK) Limited in the UK
Cardiac/peripheral vascular guidewire, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 79494. The device is manufactured by Brivant Limited T/A Lake Region Medical from Ireland, classified as Active implantable device (Directive 90/385/EEC only). The authorized representative in the UK is Emergo Consulting (UK) Limited .
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