United Kingdom MHRA device registration 160423

Monkeypox virus antigen IVD, kit, rapid ICT, clinical

United Kingdom·In Vitro Diagnostic Device·Maya Astra Technology Co., Ltd·Registered Nov 26, 2024

Registration details

Device ID: 160423
MHRA Reference Number: 160423
Date Registered: Nov 26, 2024
Last Updated: Jan 25, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Monkeypox virus antigen IVD, kit, rapid ICT, clinical
Type: IVD General

Manufacturer

Name: Maya Astra Technology Co., Ltd
Address: No. 16 Chunleilu, Xishan
Wuxi, Jiangsu, China
Created Date: Nov 11, 2022

Authorized Representative

Name: KINGSMEAD SERVICE LIMITED
Relationship Type: UK Responsible Person
Address: 19 MEZZANINE FLOOR 19-21 CRAWFORD STREET
London, England, United Kingdom
Postcode: W1H 1PJ

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About this record

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.

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