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.
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
Address
No. 680, Lusong Road, Yuelu District
Changsha , Hunan Province , China
Created Date
Aug 24, 2021
Name
Obelis UK LtdRelationship Type
Address
Sandford Gate, East Point Business Park
Oxford , England, United Kingdom
Postcode: OX4 6LB
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