Internal defibrillation electrode, adult, reusable - UK MHRA Medical Device Registration

Internal defibrillation electrode, adult, reusable is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 68357. 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.

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Internal defibrillation electrode, adult, reusable

MHRA Device ID: 68357•Ref: 68357

Device Type

General Medical Device

Devices

Internal defibrillation electrode, adult, reusable

Type

Class III

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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Internal defibrillation electrode, adult, reusable - UK MHRA Medical Device Registration

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Date Registered

Last Updated

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Created Date

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Address

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