United Kingdom MHRA device registration 179330

Evacuated blood collection tube IVD, anticoagulant/nucleic acid stabilizer

United Kingdom·In Vitro Diagnostic Device·BGI Europe A/S·Registered Nov 26, 2024

Registration details

Device ID: 179330
MHRA Reference Number: 179330
Date Registered: Nov 26, 2024
Last Updated: Oct 8, 2023

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Evacuated blood collection tube IVD, anticoagulant/nucleic acid stabilizer
Type: Class A

Manufacturer

Name: BGI Europe A/S
Address: Symfonivej 34
Herlev, Denmark
Created Date: Aug 30, 2021

Authorized Representative

Name: SUNGO Certification Company Limited
Relationship Type: UK Responsible Person
Address: 3rd Floor, 70 Gracechurch Street
London, England, United Kingdom
Postcode: EC3V 0HR

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About this record

Evacuated blood collection tube IVD, anticoagulant/nucleic acid stabilizer is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 179330. The device is manufactured by BGI Europe A/S from Denmark, classified as In Vitro Diagnostic Device. The authorized representative in the UK is SUNGO Certification Company Limited.

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