Manual endodontic file/rasp, reusable - UK MHRA Medical Device Registration
Manual endodontic file/rasp, reusable is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 178476. The device is manufactured by Foshan RIXI Medical Equipment Co., Ltd from China, classified as General Medical Device. The authorized representative in the UK is SUNGO Certification Company Limited.
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
Manual endodontic file/rasp, reusable
Type
Class I
Date Registered
Aug 25, 2024
Last Updated
Oct 8, 2023
Address
3rd Floor, Stairway A, Block 6, Guangdong New Light Source Industry Base core area within the C Zone, Foshan
Guangdong Province, China
Created Date
Sep 7, 2023
Relationship Type
Address
3rd Floor, 70 Gracechurch Street
London, England, United Kingdom
Postcode: EC3V 0HR
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