Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system lead - UK MHRA Medical Device Registration
Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system lead is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 192090. The device is manufactured by BioWave Corporation from United States, classified as General Medical Device. The authorized representative in the UK is BioWave ltd.
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Device Type
General Medical Device
Devices
Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system lead
Type
Class IIa
Date Registered
Sep 23, 2024
Last Updated
Jun 21, 2024
Address
8 Knight Street Suite 201
Norwalk, connecticut, United States
Created Date
Apr 24, 2024
Name
BioWave ltdRelationship Type
Address
1-3 college yard
worcester , England, United Kingdom
Postcode: WR1 2LA
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