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

External defibrillation electrode, adult, reusable is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 97352. The device is manufactured by Philips Medical Systems from United States, classified as General Medical Device. The authorized representative in the UK is Philips Electronics UK Ltd.

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External defibrillation electrode, adult, reusable

MHRA Device ID: 97352•Ref: 97352

Device Type

General Medical Device

Devices

External defibrillation electrode, adult, reusable

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Jun 20, 2024

Manufacturer Information

Name

Philips Medical Systems

Address

22100 Bothell Everett Highway

Bothell, WA, United States

Created Date

Aug 23, 2021

Authorized Representative

Name

Philips Electronics UK Ltd

Relationship Type

UK Responsible Person

Address

Ascent 1 Farnborough Aerospace Centre

Farnborough, Hampshire, England, United Kingdom

Postcode: GU14 6XW

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

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