Progesterone IVD, reagent - UK MHRA Medical Device Registration

Progesterone IVD, reagent is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 160855. The device is manufactured by VivaChek Biotech (Hangzhou) Co., Ltd. from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is lotus global co ltd.

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Progesterone IVD, reagent

MHRA Device ID: 160855•Ref: 160855

Device Type

In Vitro Diagnostic Device

Devices

Progesterone IVD, reagent

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Jun 11, 2024

Manufacturer Information

Name

VivaChek Biotech (Hangzhou) Co., Ltd.

Address

Level 2, Block 2, 146 East Chaofeng Rd., Yuhang Economy Development Zone,

Hangzhou, Zhejiang, China

Created Date

Mar 14, 2021

Authorized Representative

Name

lotus global co ltd

Relationship Type

UK Responsible Person

Address

23 Maine Street

Reading, Reading, England, United Kingdom

Postcode: RG2 6AG

DJ Fang

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Other Products from VivaChek Biotech (Hangzhou) Co., Ltd. (10)

Other Products from Same Authorized Representative (10)

Progesterone IVD, reagent - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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