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Fluorescent immunoassay analyser IVD, point-of-care - UK MHRA Medical Device Registration

Fluorescent immunoassay analyser IVD, point-of-care is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 176978. The device is manufactured by Vitrosens Biyoteknoloji A.S. from Turkey, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Pathaway Services Ltd.

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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Fluorescent immunoassay analyser IVD, point-of-care
MHRA Device ID: 176978โ€ขRef: 176978

Device Type

In Vitro Diagnostic Device

Devices

Fluorescent immunoassay analyser IVD, point-of-care

Type

IVD General

Date Registered

Feb 23, 2024

Last Updated

Jan 11, 2024

Manufacturer Information

Address

Serifali Mah Sehit Sokak No: 17/A

Istanbul, Umraniye, Turkey

Created Date

Jul 17, 2023

Authorized Representative

Relationship Type

UK Responsible Person

Address

Headlands House 1 Kings Court Kettering Parkway

Kettering, Northamptonshire, England, United Kingdom

Postcode: NN15 6WJ

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