Sputum liquefaction/decontamination reagent IVD - UK MHRA Medical Device Registration

Sputum liquefaction/decontamination reagent IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 87914. The device is manufactured by Copan Italia S.p.A. from Italy, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Qserve Group UK, Ltd. .

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Sputum liquefaction/decontamination reagent IVD

MHRA Device ID: 87914•Ref: 87914

Device Type

In Vitro Diagnostic Device

Devices

Sputum liquefaction/decontamination reagent IVD

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Name

Copan Italia S.p.A.

Address

Via F. Perotti 10

Brescia, Italy

Created Date

Jul 8, 2021

Authorized Representative

Name

Qserve Group UK, Ltd.

Relationship Type

UK Responsible Person

Address

49 Greek Street

London, England, United Kingdom

Postcode: W1D 4EG

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Sputum liquefaction/decontamination reagent IVD - UK MHRA Medical Device Registration

Device Type

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Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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