Cytological centrifuge funnel IVD - UK MHRA Medical Device Registration

Cytological centrifuge funnel IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 181461. The device is manufactured by ELITech Group Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is MT Promedt Consulting 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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Cytological centrifuge funnel IVD

MHRA Device ID: 181461•Ref: 181461

Device Type

In Vitro Diagnostic Device

Devices

Cytological centrifuge funnel IVD

Type

Class A

Date Registered

Nov 26, 2024

Last Updated

Jun 11, 2024

Manufacturer Information

Name

ELITech Group Inc.

Address

370 West 1700 South

Logan, Utah, United States

Created Date

Aug 17, 2021

Authorized Representative

Name

MT Promedt Consulting Ltd

Relationship Type

UK Responsible Person

Address

Beaver House, 23-38 Hythe Bridge Street

Oxford, England, United Kingdom

Postcode: OX1 2EP

DJ Fang

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Cytological centrifuge funnel IVD - UK MHRA Medical Device Registration

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Last Updated

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Address

Created Date

Name

Relationship Type

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DJ Fang

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