Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system lead
United Kingdom·General Medical Device·BioWave Corporation·Registered Sep 23, 2024- Device ID
- 192090
- MHRA Reference Number
- 192090
- Date Registered
- Sep 23, 2024
- Last Updated
- Jun 21, 2024
- Device Type
- General Medical Device
- Devices
- Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system lead
- Type
- Class IIa
- Address
- 8 Knight Street Suite 201 Norwalk, connecticut, United States
- Created Date
- Apr 24, 2024
- Name
- BioWave ltd
- Relationship Type
- UK Responsible Person
- Address
- 1-3 college yard worcester , England, United KingdomPostcode: WR1 2LA
Devices with a matching generic name or device type registered with MHRA
Additional devices registered by the same manufacturer
Additional devices represented by BioWave ltd in the UK
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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