United Kingdom MHRA device registration 173788

Coagulation analyser IVD, point-of-care, line-powered

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

Registration details

Device ID: 173788
MHRA Reference Number: 173788
Date Registered: Nov 26, 2024
Last Updated: Mar 26, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Coagulation analyser IVD, point-of-care, line-powered
Type: IVD General

Manufacturer

Name: Entegrion, Inc.
Address: 4819 Emperor Boulevard, Suite 400 4819 Emperor Boulevard, Suite 400
Durham, United States
Created Date: Jun 9, 2023

Authorized Representative

Name: Obelis UK Ltd
Relationship Type: UK Responsible Person
Address: Sandford Gate, East Point Business Park
Oxford , England, United Kingdom
Postcode: OX4 6LB

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About this record

Coagulation analyser IVD, point-of-care, line-powered is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 173788. The device is manufactured by Entegrion, Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Obelis UK Ltd.

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