Earmould, preformed - UK MHRA Medical Device Registration
Earmould, preformed is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 146931. The device is manufactured by Cochlear Europe Ltd from England, United Kingdom, classified as General Medical Device.
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Device Type
General Medical Device
Devices
Earmould, preformed
Type
Class I
Date Registered
Apr 28, 2021
Last Updated
Feb 3, 2024
Address
6 Dashwood Lang Road Bourne Business Park
Addlestone, Surrey, England, United Kingdom
Created Date
Feb 24, 2021
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