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 162289. The device is manufactured by Latvia MGI Tech SIA from Latvia, classified as In Vitro Diagnostic Device. The authorized representative in the UK is PureUKCA 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
Nucleic acid sequence analyser IVD, next-generation sequencing (NGS)
Type
Class A
Date Registered
Nov 26, 2024
Last Updated
Jan 24, 2024
Address
Mฤrupes nov., Mฤrupes pag., "Lidostas parks"
Riga, Latvia
Created Date
Dec 6, 2022
Name
PureUKCA LtdRelationship Type
Address
59 St. Martin's Lane
London, Middlesex, England, United Kingdom
Postcode: WC2N 4JS
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