Progesterone IVD, kit, chemiluminescent immunoassay - UK MHRA Medical Device Registration

Progesterone IVD, kit, chemiluminescent immunoassay is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 159459. The device is manufactured by Nanjing Poclight Biotechnology Co., Ltd. from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is HUMISS COMPANY LIMITED.

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Progesterone IVD, kit, chemiluminescent immunoassay

MHRA Device ID: 159459•Ref: 159459

Device Type

In Vitro Diagnostic Device

Devices

Progesterone IVD, kit, chemiluminescent immunoassay

Type

IVD General

Date Registered

Nov 1, 2022

Last Updated

Dec 22, 2022

Manufacturer Information

Name

Nanjing Poclight Biotechnology Co., Ltd.

Address

South Side, 2nd Floor, Building A02, Biopharmaceutical Valley Accelerator (Phase III), No. 142 Huakang Road, Jiangbei New District

Nanjing City, Jiangsu Province, China

Created Date

Nov 1, 2022

Authorized Representative

Name

HUMISS COMPANY LIMITED

Relationship Type

UK Responsible Person

Address

Suite 145 82-84 Bell Yard

London, England, United Kingdom

Postcode: WC2A 2JR

DJ Fang

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Progesterone IVD, kit, chemiluminescent immunoassay - UK MHRA Medical Device Registration

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