United Kingdom MHRA device registration 78792
Spinal procedural guidewire
United Kingdom·Active implantable device (Directive 90/385/EEC only)·St. Jude Medical·Registered Apr 6, 2021Registration details
- Device ID
- 78792
- Date Registered
- Apr 6, 2021
- Last Updated
- Dec 22, 2022
Device classification
- Device Type
- Active implantable device (Directive 90/385/EEC only)
- Devices
- Spinal procedural guidewire
- Type
- Active implantable Medical device
Manufacturer
- Name
- St. Jude Medical
- Address
- 6901 Preston Road Plano, Texas, United States
- Created Date
- Apr 6, 2021
Authorized Representative
- Relationship Type
- UK Responsible Person
- Address
- Elder House Central Boulevard Blythe Valley Business Park Solihull, West Midlands, England, United KingdomPostcode: B90 8AJ
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About this record
Spinal procedural guidewire is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 78792. The device is manufactured by St. Jude Medical from United States, classified as Active implantable device (Directive 90/385/EEC only). The authorized representative in the UK is Abbott Medical UK Limited.
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