Legionella pneumophila antigen IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration

Legionella pneumophila antigen IVD, kit, rapid ICT, clinical is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 85111. The device is manufactured by Trinity Biotech Plc from Ireland, classified as In Vitro Diagnostic Device. The authorized representative in the UK is IVDeology UKRP Ltd.

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Legionella pneumophila antigen IVD, kit, rapid ICT, clinical

MHRA Device ID: 85111•Ref: 85111

Device Type

In Vitro Diagnostic Device

Devices

Legionella pneumophila antigen IVD, kit, rapid ICT, clinical

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Apr 10, 2024

Manufacturer Information

Name

Trinity Biotech Plc

Address

IDA Business Park Southern Cross Road

Bray, Co. Wicklow, Ireland

Created Date

Jun 11, 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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Legionella pneumophila antigen IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration

Device Type

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Date Registered

Last Updated

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Created Date

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Address

DJ Fang

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