Tissue specimen MRI system container IVD - UK MHRA Medical Device Registration

Tissue specimen MRI system container IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 162239. The device is manufactured by ClearCut Medical Ltd from Israel, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Medimap Ltd.

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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Tissue specimen MRI system container IVD

MHRA Device ID: 162239•Ref: 162239

Device Type

In Vitro Diagnostic Device

Devices

Tissue specimen MRI system container IVD

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Mar 23, 2024

Manufacturer Information

Name

ClearCut Medical Ltd

Address

5 Fikes Street

Rehovot, Israel

Created Date

Oct 4, 2022

Authorized Representative

Name

Medimap Ltd

Relationship Type

UK Responsible Person

Address

2 The Drift

Thurston, Suffolk, United Kingdom

Postcode: IP31 3RT

DJ Fang

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Other Products from ClearCut Medical Ltd (2)

Tissue specimen MRI system IVD

Type: In Vitro Diagnostic Device

Registered: Nov 26, 2024

General specimen container IVD, no additive/medium

Type: In Vitro Diagnostic Device

Registered: Nov 26, 2024

Other Products from Same Authorized Representative (10)

Tissue specimen MRI system container IVD - 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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Tissue specimen MRI system IVD

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