Nasal file/rasp - UK MHRA Medical Device Registration
Nasal file/rasp is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 178868. The device is manufactured by Moses Enterprises 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
Nasal file/rasp
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
Jul 17, 2024
Relationship Type
Address
Office 32 19-21 Crawford Street
London, United Kingdom
Postcode: W1H 1PJ
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