Cancer risk assessment interpretive software IVD - UK MHRA Medical Device Registration

Cancer risk assessment interpretive software IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 182390. The device is manufactured by Veracyte Diagnostics LLC from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is UKCApartner4U 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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Cancer risk assessment interpretive software IVD

MHRA Device ID: 182390•Ref: 182390

Device Type

In Vitro Diagnostic Device

Devices

Cancer risk assessment interpretive software IVD

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Nov 19, 2024

Manufacturer Information

Name

Veracyte Diagnostics LLC

Address

6000 Shoreline Court Suite 300

South San Francisco, California, United States

Created Date

Mar 16, 2022

Authorized Representative

Name

UKCApartner4U Limited

Relationship Type

UK Responsible Person

Address

7 CAMPION WAY

BINGHAM, NOTTINGHAM, England, United Kingdom

Postcode: NG13 8 TR

DJ Fang

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Cancer risk assessment interpretive software IVD - UK MHRA Medical Device Registration

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