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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 97696. The device is manufactured by Sansure Biotech Inc. from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Obelis 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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General specimen container IVD, additive/medium
MHRA Device ID: 97696โ€ขRef: 97696

Device Type

In Vitro Diagnostic Device

Devices

General specimen container IVD, additive/medium

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Nov 9, 2024

Manufacturer Information

Address

No. 680, Lusong Road, Yuelu District

Changsha , Hunan Province , China

Created Date

Aug 24, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

Sandford Gate, East Point Business Park

Oxford , England, United Kingdom

Postcode: OX4 6LB

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