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 97348. 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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Device Type
General Medical Device
Devices
Internal defibrillation electrode, adult, reusable
Type
Class IIb
Date Registered
Nov 26, 2024
Last Updated
Jun 20, 2024
Address
22100 Bothell Everett Highway
Bothell, WA, United States
Created Date
Aug 23, 2021
Relationship Type
Address
Ascent 1 Farnborough Aerospace Centre
Farnborough, Hampshire, England, United Kingdom
Postcode: GU14 6XW
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