Manual endodontic file/rasp, single-use - UK MHRA Medical Device Registration
Manual endodontic file/rasp, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 102740. The device is manufactured by Shenzhen Perfect Medical Instruments 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, single-use
Type
Class IIa
Date Registered
Sep 4, 2021
Last Updated
Oct 8, 2023
Address
1st Floor, Building C, No. 3 Jixia Zao He Keng Industrial Zone Nanwan Road, Longgang District, Shenzhen
Guangdong Province, China
Created Date
Sep 4, 2021
Relationship Type
Address
3rd Floor, 70 Gracechurch Street
London, England, United Kingdom
Postcode: EC3V 0HR
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