United Kingdom MHRA device registration 88252

Ketamine/ketamine metabolite IVD, control

United Kingdom·In Vitro Diagnostic Device·UTAK Laboratories Inc.·Registered Nov 26, 2024

Registration details

Device ID: 88252
MHRA Reference Number: 88252
Date Registered: Nov 26, 2024
Last Updated: May 14, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Ketamine/ketamine metabolite IVD, control
Type: IVD General

Manufacturer

Name: UTAK Laboratories Inc.
Address: 25020 Avenue Tibbitts Valencia
CA, United States
Created Date: Jul 9, 2021

Authorized Representative

Name: IVDeology UKRP Ltd
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

Ketamine/ketamine metabolite IVD, control is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 88252. 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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