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 91367. The device is manufactured by Medtronic, Inc from United States, classified as General Medical Device. The authorized representative in the UK is Medtronic Limited.

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Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system pulse generator

MHRA Device ID: 91367•Ref: 91367

Device Type

General Medical Device

Devices

Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system pulse generator

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Dec 16, 2023

Manufacturer Information

Name

Medtronic, Inc

Address

710 Medtronic Parkway

Minneapolis, MN, United States

Created Date

Feb 2, 2021

Authorized Representative

Name

Medtronic Limited

Relationship Type

UK Responsible Person

Address

Building 9 Croxley Park

Watford, Herts, England, United Kingdom

Postcode: WD18 8WW

DJ Fang

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Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system pulse generator - 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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