United Kingdom MHRA device registration 210683

Progesterone IVD, kit, rapid ICT, clinical

United Kingdom·In Vitro Diagnostic Device·SD Biosensor, Inc.·Registered Feb 14, 2025DREGIY

Registration details

Device ID: 210683
Status: DREGIY
Date Registered: Feb 14, 2025

Device classification

Device Type: In Vitro Diagnostic Device
Type: IVD General

Manufacturer

Name: SD Biosensor, Inc.
Address: C-4th&5th, 16 Deogyeong-daero 1556beon-gil, Yeongtong-gu, Suwon-si, Gyeonggi-do 16690, Republic of Korea
Suwon-si, South Korea

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About this record

Progesterone IVD, kit, rapid ICT, clinical is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 210683. The device is manufactured by SD Biosensor, Inc. from South Korea, classified as In Vitro Diagnostic Device.

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