United Kingdom MHRA device registration 143461
Neurosurgical procedure kit, non-medicated, single-use
United Kingdom·Active implantable device (Directive 90/385/EEC only)·Stimwave Technologies Incorporated·Registered Apr 5, 2022Registration details
- Device ID
- 143461
- Date Registered
- Apr 5, 2022
- Last Updated
- Dec 22, 2022
Device classification
- Device Type
- Active implantable device (Directive 90/385/EEC only)
- Devices
- Neurosurgical procedure kit, non-medicated, single-use
- 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 KingdomPostcode: CB24 9BZ
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About this record
Neurosurgical procedure kit, non-medicated, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 143461. 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.
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