United Kingdom MHRA device registration 188021

Manual endodontic file/rasp, single-use

United Kingdom·General Medical Device·Shenzhen Perfect Medical Instruments Co., Ltd.·Registered Nov 26, 2024

Registration details

Device ID: 188021
MHRA Reference Number: 188021
Date Registered: Nov 26, 2024
Last Updated: Jul 31, 2024

Device classification

Device Type: General Medical Device
Devices: Manual endodontic file/rasp, single-use
Type: Class IIa

Manufacturer

Name: Shenzhen Perfect Medical Instruments Co., Ltd.
Address: Room 103, Building 3, No. 2, Weiqun Road, 4th Community, Henggang Street, Longgang District, Shenzhen
Guangdong Province, China
Created Date: Sep 4, 2021

Authorized Representative

Name: SUNGO Certification Company Limited
Relationship Type: UK Responsible Person
Address: 3rd Floor, 70 Gracechurch Street
London, England, United Kingdom
Postcode: EC3V 0HR

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About this record

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 188021. 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.

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