Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system pulse generator - UK MHRA Medical Device Registration
Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system pulse generator is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 145561. The device is manufactured by Nevro Corporation from United States, classified as Active implantable device (Directive 90/385/EEC only). The authorized representative in the UK is MDSS-UK RP LIMITED.
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Device Type
Active implantable device (Directive 90/385/EEC only)
Devices
Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system pulse generator
Type
Active implantable Medical device
Date Registered
Jun 22, 2021
Last Updated
Dec 22, 2022
Address
1800 Bridge Parkway
Redwood City, CA, United States
Created Date
Jun 22, 2021
Relationship Type
Address
6 Wilmslow Road, Rusholme
Manchester, England, United Kingdom
Postcode: M14 5TP
Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system pulse generator
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Manufacturer: Medtronic, Inc
Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system pulse generator
Type: Active Implantable Device
Manufacturer: Boston Scientific Neuromodulation Corporation
Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system pulse generator
Type: General Medical Device
Manufacturer: Medtronic, Inc
Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system pulse generator
Type: Active Implantable Device
Manufacturer: Abbott Medical
Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system pulse generator
Type: General Medical Device
Manufacturer: Nevro Corporation
Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system pulse generator
Type: General Medical Device
Manufacturer: Nevro Corporation
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Type: Active implantable device (Directive 90/385/EEC only)
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Type: Active implantable device (Directive 90/385/EEC only)
Manufacturer: Stimwave Technologies Incorporated
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Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system pulse generator
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Registered: Jun 22, 2024
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