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 93579. The device is manufactured by ZOLL Medical Corporation from United States, classified as General Medical Device. The authorized representative in the UK is ZOLL Medical 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, paediatric, single-use

MHRA Device ID: 93579•Ref: 93579

Device Type

General Medical Device

Devices

External defibrillation electrode, paediatric, single-use

Type

Class IIb

Date Registered

Nov 22, 2024

Last Updated

Nov 2, 2024

Manufacturer Information

Name

ZOLL Medical Corporation

Address

269 Mill Road

Chelmsford, MA, United States

Created Date

Mar 19, 2021

Authorized Representative

Name

ZOLL Medical UK Ltd

Relationship Type

UK Responsible Person

Address

9 Seymour Court Tudor Road Manor Park

Runcorn, Cheshire, England, United Kingdom

Postcode: WA7 1SY

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

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

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