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 204907. The device is manufactured by Accucise Diagnostics Inc. from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is SUNGO Certification Company Limited.

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Progesterone IVD, kit, chemiluminescent immunoassay

MHRA Device ID: 204907•Ref: 204907

Device Type

In Vitro Diagnostic Device

Devices

Progesterone IVD, kit, chemiluminescent immunoassay

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Nov 14, 2024

Manufacturer Information

Name

Accucise Diagnostics Inc.

Address

Suite 501&601, Building 9, Medpark, 188 Fuchunjiang Rd., SND

Suzhou Province, China

Created Date

Nov 8, 2024

Authorized Representative

Name

SUNGO Certification Company Limited

Relationship Type

UK Responsible Person

Address

3rd Floor, 70 Gracechurch Street

London, England, United Kingdom

Postcode: EC3V 0HR

DJ Fang

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

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Address

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