External defibrillation electrode, adult, single-use - UK MHRA Medical Device Registration

External defibrillation electrode, adult, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 95349. 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.

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External defibrillation electrode, adult, single-use

MHRA Device ID: 95349•Ref: 95349

Device Type

General Medical Device

Devices

External defibrillation electrode, adult, single-use

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Aug 13, 2024

Manufacturer Information

Name

Defibtech, LLC

Address

Boston Post Road 741

Guilford, United States

Created Date

Aug 17, 2021

Authorized Representative

Name

NIHONKOHDEN UK LTD

Relationship Type

UK Responsible Person

Address

Unit 3, Heyworth Business Park Old Portsmouth Road, Peasmarsh GUILDFORD

GUILDFORD, Surrey, England, United Kingdom

Postcode: GU3 1AF

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External defibrillation electrode, adult, single-use - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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