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Multiple Aspergillus species antigen IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

Multiple Aspergillus species antigen IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 147833. The device is manufactured by Pearl Diagnostics, Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Emergo Consulting (UK) 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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Multiple Aspergillus species antigen IVD, kit, enzyme immunoassay (EIA)
MHRA Device ID: 147833โ€ขRef: 147833

Device Type

In Vitro Diagnostic Device

Devices

Multiple Aspergillus species antigen IVD, kit, enzyme immunoassay (EIA)

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Sep 10, 2024

Manufacturer Information

Address

1812 Ashland Ave Suite G32

Baltimore, Maryland, United States

Created Date

May 20, 2022

Authorized Representative

Relationship Type

UK Responsible Person

Address

Compass House, Vision Park Histon c/o Cr360 โ€“ UL International

Cambridge, England, United Kingdom

Postcode: CB24 9BZ

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