Mycoplasma pneumoniae immunoglobulin A (IgA) antibody IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

Mycoplasma pneumoniae immunoglobulin A (IgA) antibody IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 114350. The device is manufactured by Diesse Diagnostica Senese Spa from Italy, classified as In Vitro Diagnostic Device. The authorized representative in the UK is IVDeology UKRP Ltd.

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Mycoplasma pneumoniae immunoglobulin A (IgA) antibody IVD, kit, enzyme immunoassay (EIA)

MHRA Device ID: 114350•Ref: 114350

Device Type

In Vitro Diagnostic Device

Devices

Mycoplasma pneumoniae immunoglobulin A (IgA) antibody IVD, kit, enzyme immunoassay (EIA)

Type

IVD General

Date Registered

Nov 22, 2024

Last Updated

Oct 25, 2024

Manufacturer Information

Name

Diesse Diagnostica Senese Spa

Address

Diesse Diagnostica Senese Spa Viale Decumano 36

Milan, Italy

Created Date

Jul 8, 2021

Authorized Representative

Name

IVDeology UKRP Ltd

Relationship Type

UK Responsible Person

Address

Maidstone Innovation Centre Gidds Pond Way

Maidstone, Kent, England, United Kingdom

Postcode: ME14 5FY

DJ Fang

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Mycoplasma pneumoniae immunoglobulin A (IgA) antibody IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

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