User-induced pipette - UK MHRA Medical Device Registration

User-induced pipette is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 144748. The device is manufactured by Kirgen Bioscience (Hainan) Co., Ltd from China, classified as General Medical Device. The authorized representative in the UK is SUNGO Certification Company Limited.

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User-induced pipette

MHRA Device ID: 144748•Ref: 144748

Device Type

General Medical Device

Devices

User-induced pipette

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Oct 8, 2023

Manufacturer Information

Name

Kirgen Bioscience (Hainan) Co., Ltd

Address

3-7A, American Industry Park, 100 Nanhai Avenue, Haikou City

Hainan Province, China

Created Date

Apr 15, 2022

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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User-induced pipette - UK MHRA Medical Device Registration

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