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United Kingdom MHRA device registration 210361

Nucleic acid hybridization detection IVD, reagent

United Kingdom flagUnited Kingdom·In Vitro Diagnostic Device·Agilent Technologies, Inc. ·Registered Feb 8, 2025DREGIY
Registration details
Device ID
210361
Status
DREGIY
Date Registered
Feb 8, 2025
Device classification
Device Type
In Vitro Diagnostic Device
Type
Class A
Manufacturer
Name
Agilent Technologies, Inc.
Address
5301 Stevens Creek Blvd
Santa Clara, California , United States
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About this record

Nucleic acid hybridization detection IVD, reagent is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 210361. The device is manufactured by Agilent Technologies, Inc. from United States, classified as In Vitro Diagnostic Device.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, 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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