United Kingdom MHRA device registration 97352

External defibrillation electrode, adult, reusable

United Kingdom·General Medical Device·Philips Medical Systems·Registered Nov 26, 2024

Registration details

Device ID: 97352
MHRA Reference Number: 97352
Date Registered: Nov 26, 2024
Last Updated: Jun 20, 2024

Device classification

Device Type: General Medical Device
Devices: External defibrillation electrode, adult, reusable
Type: Class IIb

Manufacturer

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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About this record

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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