Manual goniometer - UK MHRA Medical Device Registration
Manual goniometer is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 152521. The device is manufactured by Fabrication Enterprises, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is AJW Technology Consulting Ltd.
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Device Type
General Medical Device
Devices
Manual goniometer
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
Jan 16, 2024
Address
250 Clearbrook Rd.
Elmsford, New York, United States
Created Date
Jul 7, 2022
Relationship Type
Address
4/4a Bloomsbury Square
London, England, United Kingdom
Postcode: WC1A 2RP
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