Nucleic acid sequence analyser IVD, next-generation sequencing (NGS) - UK MHRA Medical Device Registration
Nucleic acid sequence analyser IVD, next-generation sequencing (NGS) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 139849. The device is manufactured by Tempus AI, Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is MDSS-UK RP 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
In Vitro Diagnostic Device
Devices
Nucleic acid sequence analyser IVD, next-generation sequencing (NGS)
Type
IVD General
Date Registered
Nov 26, 2024
Last Updated
Mar 23, 2024
Name
Tempus AI, Inc.Address
600 W Chicago Ave, Suite 510
Chicago, IL, United States
Created Date
Mar 14, 2022
Relationship Type
Address
6 Wilmslow Road, Rusholme
Manchester, England, United Kingdom
Postcode: M14 5TP
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