Tissue embedding mould IVD, reusable - UK MHRA Medical Device Registration

Tissue embedding mould IVD, reusable is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 135021. The device is manufactured by Sakura Finetek USA, Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Qserve Group UK, 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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In Vitro Diagnostic Device

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Tissue embedding mould IVD, reusable

MHRA Device ID: 135021•Ref: 135021

Device Type

In Vitro Diagnostic Device

Devices

Tissue embedding mould IVD, reusable

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Name

Sakura Finetek USA, Inc.

Address

1750 West 214th Street

Torrance, California , United States

Created Date

Feb 3, 2022

Authorized Representative

Name

Qserve Group UK, Ltd.

Relationship Type

UK Responsible Person

Address

49 Greek Street

London, England, United Kingdom

Postcode: W1D 4EG

DJ Fang

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Other Products from Sakura Finetek USA, Inc. (6)

Other Products from Same Authorized Representative (10)

Tissue embedding mould IVD, reusable - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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