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 162008. The device is manufactured by Cochlear Ltd from Australia, classified as General Medical Device. The authorized representative in the UK is Cochlear Europe Ltd.

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Earmould, preformed

MHRA Device ID: 162008•Ref: 162008

Device Type

General Medical Device

Devices

Earmould, preformed

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Mar 1, 2024

Manufacturer Information

Name

Cochlear Ltd

Address

1 University Avenue Macquarie University

Sydney, NSW, Australia

Created Date

Apr 28, 2021

Authorized Representative

Name

Cochlear Europe Ltd

Relationship Type

UK Responsible Person

Address

6 Dashwood Lang Road Bourne Business Park

Addlestone, Surrey, England, United Kingdom

Postcode: KT15 2HJ

DJ Fang

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Other Products from Cochlear Ltd (10)

Other Products from Same Authorized Representative (10)

Earmould, preformed - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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