Middle ear file/rasp - UK MHRA Medical Device Registration
Middle ear file/rasp is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 106364. The device is manufactured by PHEASANT SURGICAL CORPORATION from Pakistan, classified as General Medical Device. The authorized representative in the UK is CMC Medical Devices LTD.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Device Type
General Medical Device
Devices
Middle ear file/rasp
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
Jun 6, 2024
Address
786 # NAI ABADI MURAD PUR
SIALKOT, Pakistan
Created Date
Aug 15, 2021
Relationship Type
Address
Office 32 19-21 Crawford Street
London, United Kingdom
Postcode: W1H 1PJ
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