United Kingdom MHRA device registration 95335

Osmolality IVD, control

United Kingdom·In Vitro Diagnostic Device·ELITech Group Inc.·Registered Nov 26, 2024

Registration details

Device ID: 95335
MHRA Reference Number: 95335
Date Registered: Nov 26, 2024
Last Updated: Jun 11, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Osmolality IVD, control
Type: IVD General

Manufacturer

Name: ELITech Group Inc.
Address: 370 West 1700 South
Logan, Utah, United States
Created Date: Aug 17, 2021

Authorized Representative

Name: MT Promedt Consulting Ltd
Relationship Type: UK Responsible Person
Address: Beaver House, 23-38 Hythe Bridge Street
Oxford, England, United Kingdom
Postcode: OX1 2EP

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About this record

Osmolality IVD, control is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 95335. The device is manufactured by ELITech Group Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is MT Promedt Consulting Ltd.

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