Luteinizing hormone (LH) IVD, kit, rapid ICT, self-testing - UK MHRA Medical Device Registration

Luteinizing hormone (LH) IVD, kit, rapid ICT, self-testing is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 191422. The device is manufactured by Acon Laboratories, Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is MDSS-UK RP LIMITED.

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In Vitro Diagnostic Device

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Luteinizing hormone (LH) IVD, kit, rapid ICT, self-testing

MHRA Device ID: 191422•Ref: 191422

Device Type

In Vitro Diagnostic Device

Devices

Luteinizing hormone (LH) IVD, kit, rapid ICT, self-testing

Type

IVD Devices for Self-Testing

Date Registered

Nov 26, 2024

Last Updated

Mar 12, 2024

Manufacturer Information

Name

Acon Laboratories, Inc.

Address

5850 Oberlin Drive, #340

San Diego, CA, United States

Created Date

Mar 31, 2021

Authorized Representative

Name

MDSS-UK RP LIMITED

Relationship Type

UK Responsible Person

Address

6 Wilmslow Road, Rusholme

Manchester, England, United Kingdom

Postcode: M14 5TP

DJ Fang

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Luteinizing hormone (LH) IVD, kit, rapid ICT, self-testing - UK MHRA Medical Device Registration

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