Tympanostomy tube - UK MHRA Medical Device Registration
Tympanostomy tube is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 93089. The device is manufactured by Gyrus ACMI, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is KeyMed (Medical & Industrial Equipment) Ltd..
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Device Type
General Medical Device
Devices
Tympanostomy tube
Type
Class IIb
Date Registered
Nov 26, 2024
Last Updated
Oct 10, 2024
Name
Gyrus ACMI, Inc.Address
9600 Louisiana Ave.
North Brooklyn Park, United States
Created Date
Jul 23, 2021
Relationship Type
Address
Keymed House Stock Road
Southend-on-sea, Essex, United Kingdom
Postcode: SS2 5QH
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