Sputum liquefaction/decontamination reagent IVD - UK MHRA Medical Device Registration
Sputum liquefaction/decontamination reagent IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 139277. The device is manufactured by Alpha-Tec Systems, 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
Sputum liquefaction/decontamination reagent IVD
Type
IVD General
Date Registered
Nov 26, 2024
Last Updated
Oct 10, 2023
Address
1311 SE Cardinal Court, Suite 170
Vancouver, WA, United States
Created Date
Mar 8, 2022
Relationship Type
Address
6 Wilmslow Road, Rusholme
Manchester, England, United Kingdom
Postcode: M14 5TP
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