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Hepatitis B virus e-antigen IVD, kit, chemiluminescent immunoassay - UK MHRA Medical Device Registration

Hepatitis B virus e-antigen IVD, kit, chemiluminescent immunoassay is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 210170. The device is manufactured by DiaSorin Italia S.p.A. from Italy, classified as In Vitro Diagnostic Device.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, 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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Hepatitis B virus e-antigen IVD, kit, chemiluminescent immunoassay
MHRA Device ID: 210170

Device Type

In Vitro Diagnostic Device

Type

Class D

Status

DREGIY

Date Registered

Feb 6, 2025

Manufacturer Information

Address

Via Crescentino, snc

Saluggia, VC, Italy

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