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 68360. The device is manufactured by Physio-Control, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is Stryker 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: 68360•Ref: 68360

Device Type

General Medical Device

Devices

External defibrillation electrode, paediatric, single-use

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Name

Physio-Control, Inc.

Address

11811 Willow Road

NE Redmond, Washington, United States

Created Date

Mar 3, 2021

Authorized Representative

Name

Stryker UK Ltd

Relationship Type

UK Responsible Person

Address

Stryker House Hambridge Road

Newbury, Berkshire, England, United Kingdom

Postcode: RG14 5AW

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

Device Type

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Type

Date Registered

Last Updated

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Address

Created Date

Name

Relationship Type

Address

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