Monkeypox virus antigen IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration
Monkeypox virus antigen IVD, kit, rapid ICT, clinical is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 160423. The device is manufactured by Maya Astra Technology Co., Ltd from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is KINGSMEAD SERVICE 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
Monkeypox virus antigen IVD, kit, rapid ICT, clinical
Type
IVD General
Date Registered
Nov 26, 2024
Last Updated
Jan 25, 2024
Address
No. 16 Chunleilu, Xishan
Wuxi, Jiangsu, China
Created Date
Nov 11, 2022
Relationship Type
Address
19 MEZZANINE FLOOR 19-21 CRAWFORD STREET
London, England, United Kingdom
Postcode: W1H 1PJ
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