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Evacuated blood collection tube IVD, anticoagulant/nucleic acid stabilizer - UK MHRA Medical Device Registration

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.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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In Vitro Diagnostic Device
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Evacuated blood collection tube IVD, anticoagulant/nucleic acid stabilizer
MHRA Device ID: 179330โ€ขRef: 179330

Device Type

In Vitro Diagnostic Device

Devices

Evacuated blood collection tube IVD, anticoagulant/nucleic acid stabilizer

Type

Class A

Date Registered

Nov 26, 2024

Last Updated

Oct 8, 2023

Manufacturer Information

Address

Symfonivej 34

Herlev, Denmark

Created Date

Aug 30, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

3rd Floor, 70 Gracechurch Street

London, England, United Kingdom

Postcode: EC3V 0HR

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