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Multi-modality clinical specimen analysis system IVD - UK MHRA Medical Device Registration

Multi-modality clinical specimen analysis system IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 170262. The device is manufactured by Guangzhou Wondfo Biotech Co., Ltd. from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Qarad UK Ltd..

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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Multi-modality clinical specimen analysis system IVD
MHRA Device ID: 170262โ€ขRef: 170262

Device Type

In Vitro Diagnostic Device

Devices

Multi-modality clinical specimen analysis system IVD

Type

IVD General

Date Registered

Jul 31, 2024

Last Updated

May 9, 2024

Manufacturer Information

Address

No.8 Lizhishan Road, Science City, Huangpu District

Guangzhou, China

Created Date

Mar 7, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

8 Northumberland Ave

Westminster, London , England, United Kingdom

Postcode: WC2N 5BY

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