External defibrillation electrode, paediatric, single-use - UK MHRA Medical Device Registration
External defibrillation electrode, paediatric, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 95348. The device is manufactured by Defibtech, LLC from United States, classified as General Medical Device. The authorized representative in the UK is NIHONKOHDEN UK LTD.
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
External defibrillation electrode, paediatric, single-use
Type
Class IIb
Date Registered
Nov 26, 2024
Last Updated
Aug 13, 2024
Relationship Type
Address
Unit 3, Heyworth Business Park Old Portsmouth Road, Peasmarsh GUILDFORD
GUILDFORD, Surrey, England, United Kingdom
Postcode: GU3 1AF
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