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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 112325. The device is manufactured by Leica Biosystems Imaging Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Leica Microsystems (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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Laboratory instrument/analyser application software IVD
MHRA Device ID: 112325โ€ขRef: 112325

Device Type

In Vitro Diagnostic Device

Devices

Laboratory instrument/analyser application software IVD

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Nov 12, 2024

Manufacturer Information

Address

1360 Park Center Drive

Vista, California, United States

Created Date

Nov 11, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

Larch House Woodlands Business Park

Milton Keynes, England, United Kingdom

Postcode: MK14 6FG

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