Implantable spinal cord electrical stimulation system programmer - UK MHRA Medical Device Registration
Implantable spinal cord electrical stimulation system programmer is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 81504. The device is manufactured by Abbott Medical from United States, classified as Active implantable device (Directive 90/385/EEC only). The authorized representative in the UK is Abbott Medical 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.
Device Type
Active implantable device (Directive 90/385/EEC only)
Devices
Implantable spinal cord electrical stimulation system programmer
Type
Active implantable Medical device
Date Registered
Mar 12, 2021
Last Updated
Dec 22, 2022
Relationship Type
Address
Elder House Central Boulevard Blythe Valley Business Park
Solihull, West Midlands, England, United Kingdom
Postcode: B90 8AJ
Implantable spinal cord electrical stimulation system programmer
Type: General Medical Device
Manufacturer: Nevro Corporation
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Type: Active implantable device (Directive 90/385/EEC only)
Manufacturer: Stimwave Technologies Incorporated
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Type: Active implantable device (Directive 90/385/EEC only)
Manufacturer: Stimwave Technologies Incorporated
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Type: Active implantable device (Directive 90/385/EEC only)
Manufacturer: Stimwave Technologies Incorporated
Soft-tissue/mesh anchor, non-bioabsorbable
Type: Active implantable device (Directive 90/385/EEC only)
Manufacturer: Stimwave Technologies Incorporated
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Type: Active implantable device (Directive 90/385/EEC only)
Manufacturer: Stimwave Technologies Incorporated
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Type: Active implantable device (Directive 90/385/EEC only)
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Type: Active implantable device (Directive 90/385/EEC only)
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Type: Active implantable device (Directive 90/385/EEC only)
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Registered: Feb 20, 2025
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Registered: Jan 31, 2025
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Registered: Jan 30, 2025
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Registered: Dec 7, 2024
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Type: System or Procedure Pack
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Type: General Medical Device
Manufacturer: Abbott Medical
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Type: General Medical Device
Manufacturer: Irvine Biomedical Inc. a St. Jude Medical Company
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Type: General Medical Device
Manufacturer: St. Jude Medical

