Follicle stimulating hormone (FSH) IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

Follicle stimulating hormone (FSH) IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 150653. The device is manufactured by VicTorch Meditek, Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is UKCApartner4U Limited.

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Follicle stimulating hormone (FSH) IVD, kit, enzyme immunoassay (EIA)

MHRA Device ID: 150653•Ref: 150653

Device Type

In Vitro Diagnostic Device

Devices

Follicle stimulating hormone (FSH) IVD, kit, enzyme immunoassay (EIA)

Type

IVD General

Date Registered

Jun 30, 2022

Last Updated

Apr 13, 2023

Manufacturer Information

Name

VicTorch Meditek, Inc.

Address

6888 Nancy Ridge Drive

San Diego, California, United States

Created Date

Jun 30, 2022

Authorized Representative

Name

UKCApartner4U Limited

Relationship Type

UK Responsible Person

Address

7 CAMPION WAY

BINGHAM, NOTTINGHAM, England, United Kingdom

Postcode: NG13 8 TR

DJ Fang

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Follicle stimulating hormone (FSH) IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

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