Urine sediment IVD, control - UK MHRA Medical Device Registration

Urine sediment IVD, control is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 131350. The device is manufactured by Kova International, Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Advena Ltd.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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In Vitro Diagnostic Device

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Urine sediment IVD, control

MHRA Device ID: 131350•Ref: 131350

Device Type

In Vitro Diagnostic Device

Devices

Urine sediment IVD, control

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Dec 20, 2023

Manufacturer Information

Name

Kova International, Inc.

Address

7272 Chapman Avenue Suite B

Garden Grove, California, United States

Created Date

Jan 7, 2022

Authorized Representative

Name

Advena Ltd

Relationship Type

UK Responsible Person

Address

Pure Offices Plato Close

Warwick, England, United Kingdom

Postcode: CV34 6WE

DJ Fang

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Urine sediment IVD, control - UK MHRA Medical Device Registration

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