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General specimen container IVD, additive/medium - UK MHRA Medical Device Registration

General specimen container IVD, additive/medium is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 132970. The device is manufactured by Hangzhou Bioer Technology Co., Ltd. from China, classified as In Vitro Diagnostic 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.

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In Vitro Diagnostic Device
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General specimen container IVD, additive/medium
MHRA Device ID: 132970โ€ขRef: 132970

Device Type

In Vitro Diagnostic Device

Devices

General specimen container IVD, additive/medium

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Aug 15, 2024

Manufacturer Information

Address

1192 BinAn Rd, Binjiang District, Hangzhou

Zhejiang Province, China

Created Date

Nov 10, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

3rd Floor, 70 Gracechurch Street

London, England, United Kingdom

Postcode: EC3V 0HR

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