Hand-held deep-tissue electromagnetic stimulator - UK MHRA Medical Device Registration
Hand-held deep-tissue electromagnetic stimulator is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 87729. The device is manufactured by BioElectronics Corporation from United States, classified as General Medical Device. The authorized representative in the UK is MDSS-UK RP 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
General Medical Device
Devices
Hand-held deep-tissue electromagnetic stimulator
Type
Class IIa
Date Registered
Nov 26, 2024
Last Updated
Apr 17, 2024
Address
4539 Metropolitan Court
Frederick, MD, United States
Created Date
Jul 6, 2021
Relationship Type
Address
6 Wilmslow Road, Rusholme
Manchester, England, United Kingdom
Postcode: M14 5TP
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