General specimen container IVD, no additive/medium - UK MHRA Medical Device Registration

General specimen container IVD, no additive/medium is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 157561. 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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General specimen container IVD, no additive/medium

MHRA Device ID: 157561•Ref: 157561

Device Type

In Vitro Diagnostic Device

Devices

General specimen container IVD, no additive/medium

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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Type: In Vitro Diagnostic Device

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Type: In Vitro Diagnostic Device

Registered: Nov 26, 2024

Other Products from Same Authorized Representative (10)

General specimen container IVD, no additive/medium - UK MHRA Medical Device Registration

Device Type

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Date Registered

Last Updated

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Created Date

Name

Relationship Type

Address

DJ Fang

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