United Kingdom MHRA device registration 88222

Methotrexate therapeutic drug monitoring IVD, control

United Kingdom flagUnited Kingdom·In Vitro Diagnostic Device·UTAK Laboratories Inc.·Registered Nov 26, 2024
Registration details
Device ID
88222
MHRA Reference Number
88222
Date Registered
Nov 26, 2024
Last Updated
May 14, 2024
Device classification
Device Type
In Vitro Diagnostic Device
Devices
Methotrexate therapeutic drug monitoring IVD, control
Type
IVD General
Manufacturer
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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About this record

Methotrexate therapeutic drug monitoring IVD, control is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 88222. 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.

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