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 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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Manual endodontic file/rasp, single-use

MHRA Device ID: 188021•Ref: 188021

Device Type

General Medical Device

Devices

Manual endodontic file/rasp, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Jul 31, 2024

Manufacturer Information

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

DJ Fang

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Other Products from Shenzhen Perfect Medical Instruments Co., Ltd. (8)

Other Products from Same Authorized Representative (10)

Manual endodontic file/rasp, single-use - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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