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Lead IVD, control - UK MHRA Medical Device Registration

Lead IVD, control is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 88226. The device is manufactured by UTAK Laboratories Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is IVDeology UKRP 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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Lead IVD, control
MHRA Device ID: 88226โ€ขRef: 88226

Device Type

In Vitro Diagnostic Device

Devices

Lead IVD, control

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

May 14, 2024

Manufacturer Information

Address

25020 Avenue Tibbitts Valencia

CA, United States

Created Date

Jul 9, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

Maidstone Innovation Centre Gidds Pond Way

Maidstone, Kent, England, United Kingdom

Postcode: ME14 5FY

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