Rotary microtome IVD - UK MHRA Medical Device Registration

Rotary microtome IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 135023. 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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Rotary microtome IVD

MHRA Device ID: 135023•Ref: 135023

Device Type

In Vitro Diagnostic Device

Devices

Rotary microtome IVD

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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Rotary microtome IVD - UK MHRA Medical Device Registration

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DJ Fang

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