United Kingdom MHRA device registration 162289

Nucleic acid sequence analyser IVD, next-generation sequencing (NGS)

United Kingdom flagUnited Kingdom·In Vitro Diagnostic Device·Latvia MGI Tech SIA·Registered Nov 26, 2024
Registration details
Device ID
162289
MHRA Reference Number
162289
Date Registered
Nov 26, 2024
Last Updated
Jan 24, 2024
Device classification
Device Type
In Vitro Diagnostic Device
Devices
Nucleic acid sequence analyser IVD, next-generation sequencing (NGS)
Type
Class A
Manufacturer
Address
Mārupes nov., Mārupes pag., "Lidostas parks"
Riga, Latvia
Created Date
Dec 6, 2022
Authorized Representative
Relationship Type
UK Responsible Person
Address
59 St. Martin's Lane
London, Middlesex, England, United Kingdom
Postcode: WC2N 4JS
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About this record

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.

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