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 132421. The device is manufactured by HiMedia Laboratories Private Ltd. from India, classified as In Vitro Diagnostic Device. The authorized representative in the UK is UKCApartner4U 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
Nov 19, 2024
Address
Plot No. C-40, Road No. 21/Y MIDC Wagle Industrial Area
Thane (West), Maharashtra, India
Created Date
Jan 14, 2022
Relationship Type
Address
7 CAMPION WAY
BINGHAM, NOTTINGHAM, England, United Kingdom
Postcode: NG13 8 TR
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