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 201900. The device is manufactured by BioWave Corporation from United States, classified as General Medical Device. The authorized representative in the UK is Obelis UK Ltd.

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Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system lead

MHRA Device ID: 201900•Ref: 201900

Device Type

General Medical Device

Devices

Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system lead

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Oct 1, 2024

Manufacturer Information

Name

BioWave Corporation

Address

3 Brooke St

Norwalk, CT, United States

Created Date

Sep 26, 2024

Authorized Representative

Name

Obelis UK Ltd

Relationship Type

UK Responsible Person

Address

Sandford Gate, East Point Business Park

Oxford , England, United Kingdom

Postcode: OX4 6LB

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Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system lead - UK MHRA Medical Device Registration

Device Type

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Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system lead

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