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.
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
User-induced pipette
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
Oct 8, 2023
Address
3-7A, American Industry Park, 100 Nanhai Avenue, Haikou City
Hainan Province, China
Created Date
Apr 15, 2022
Relationship Type
Address
3rd Floor, 70 Gracechurch Street
London, England, United Kingdom
Postcode: EC3V 0HR
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