Laboratory instrument/analyser application software IVD - UK MHRA Medical Device Registration

Laboratory instrument/analyser application software IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 169651. The device is manufactured by Proscia, Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Emergo Consulting (UK) Limited .

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Laboratory instrument/analyser application software IVD

MHRA Device ID: 169651•Ref: 169651

Device Type

In Vitro Diagnostic Device

Devices

Laboratory instrument/analyser application software IVD

Type

Class A

Date Registered

Nov 26, 2024

Last Updated

Aug 3, 2024

Manufacturer Information

Name

Proscia, Inc.

Address

1700 Market Street, Floor 24

Philadelphia, PA, United States

Created Date

Mar 29, 2023

Authorized Representative

Name

Emergo Consulting (UK) Limited

Relationship Type

UK Responsible Person

Address

Compass House, Vision Park Histon c/o Cr360 – UL International

Cambridge, England, United Kingdom

Postcode: CB24 9BZ

DJ Fang

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Laboratory instrument/analyser application software IVD - UK MHRA Medical Device Registration

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