United Kingdom MHRA device registration 143458

Spinal cord/peripheral nerve implantable analgesic electrical stimulation system programmer

United Kingdom flagUnited Kingdom·Active implantable device (Directive 90/385/EEC only)·Stimwave Technologies Incorporated·Registered Apr 5, 2022
Registration details
Device ID
143458
Date Registered
Apr 5, 2022
Last Updated
Dec 22, 2022
Device classification
Device Type
Active implantable device (Directive 90/385/EEC only)
Devices
Spinal cord/peripheral nerve implantable analgesic electrical stimulation system programmer
Type
Active implantable Medical device
Manufacturer
Address
1310 Park Central Blvd S
Pompano Beach, Florida, United States
Created Date
Apr 5, 2022
Authorized Representative
Relationship Type
UK Responsible Person
Address
Compass House, Vision Park Histon c/o Cr360 – UL International
Cambridge, England, United Kingdom
Postcode: CB24 9BZ
Similar products

Devices with a matching generic name or device type registered with MHRA

Spinal cord/peripheral nerve implantable analgesic electrical stimulation system programmerNov 6, 2024
Type: Active Implantable Device
Manufacturer: Mainstay Medical Limited
Device ID: 204699
Spinal cord/peripheral nerve implantable analgesic electrical stimulation system programmerOct 9, 2024
Type: General Medical Device
Manufacturer: Mainstay Medical Limited
Device ID: 202789
Spinal cord/peripheral nerve implantable analgesic electrical stimulation system programmerJun 22, 2024
Type: General Medical Device
Manufacturer: Nevro Corporation
Device ID: 195689
Soft-tissue/mesh anchor, non-bioabsorbableApr 5, 2022
Type: Active implantable device (Directive 90/385/EEC only)
Manufacturer: Stimwave Technologies Incorporated
Device ID: 143460
Noninvasive device battery chargerApr 5, 2022
Type: Active implantable device (Directive 90/385/EEC only)
Manufacturer: Stimwave Technologies Incorporated
Device ID: 143459
Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wireless connectionApr 5, 2022
Type: Active implantable device (Directive 90/385/EEC only)
Manufacturer: Stimwave Technologies Incorporated
Device ID: 143463
Personal device holder, reusableApr 5, 2022
Type: Active implantable device (Directive 90/385/EEC only)
Manufacturer: Stimwave Technologies Incorporated
Device ID: 143464
Spinal cord/peripheral nerve implantable analgesic electrical stimulation system external electrodeApr 5, 2022
Type: Active implantable device (Directive 90/385/EEC only)
Manufacturer: Stimwave Technologies Incorporated
Device ID: 143457
Neurosurgical procedure kit, non-medicated, single-useApr 5, 2022
Type: Active implantable device (Directive 90/385/EEC only)
Manufacturer: Stimwave Technologies Incorporated
Device ID: 143461
Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, extracorporealApr 5, 2022
Type: Active implantable device (Directive 90/385/EEC only)
Manufacturer: Stimwave Technologies Incorporated
Device ID: 143462
Other products from Stimwave Technologies Incorporated

Additional devices registered by the same manufacturer

Other products from same authorized representative

Additional devices represented by Emergo Consulting (UK) Limited in the UK

About this record

Spinal cord/peripheral nerve implantable analgesic electrical stimulation system programmer is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 143458. The device is manufactured by Stimwave Technologies Incorporated from United States, classified as Active implantable device (Directive 90/385/EEC only). The authorized representative in the UK is Emergo Consulting (UK) Limited .

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

Free DatabasePowered by Pure Global AIMHRA RegisteredActive implantable device (Directive 90/385/EEC only)