Needle guide, single-use - UK MHRA Medical Device Registration
Needle guide, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 84236. The device is manufactured by DIXI Medical from France, classified as General Medical Device. The authorized representative in the UK is Medes Ltd..
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Device Type
General Medical Device
Devices
Needle guide, single-use
Type
Class III
Date Registered
Nov 26, 2024
Last Updated
Aug 8, 2024
Name
DIXI MedicalAddress
2A route de Pouligney Chaudefontaine
Marchaux-Chaudefontaine, France
Created Date
Jun 3, 2021
Name
Medes Ltd.Relationship Type
Address
5 Beaumont Gate, Shenley Hil
Radlett, Herts, England, United Kingdom
Postcode: WD77AR
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