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 97222. The device is manufactured by Philips Goldway Shenzhen Industrial Inc. from China, 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
External defibrillation electrode, adult, reusable
Type
Class IIb
Date Registered
Nov 26, 2024
Last Updated
Jun 20, 2024
Address
No.2 Keji North 3rd Road Nanshan District
Shenzhen, China
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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