Nucleic acid amplification mastermix kit IVD - UK MHRA Medical Device Registration
Nucleic acid amplification mastermix kit IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 157797. The device is manufactured by Entrogen Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Launch Diagnostics 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 amplification mastermix kit IVD
Type
Class A
Date Registered
Jun 17, 2024
Last Updated
Apr 23, 2024
Name
Entrogen Inc.Address
Suite B 20950 Warner Center Ln Woodland Hills
Los Angeles, CA, United States
Created Date
May 17, 2021
Relationship Type
Address
Unit 20 Ash Way Thorp Arch Estate
Wetherby, England, United Kingdom
Postcode: LS23 7FA
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