Cytological centrifuge IVD - UK MHRA Medical Device Registration

Cytological centrifuge IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 163710. The device is manufactured by Sakura Seiki Co., Ltd. from Japan, 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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Cytological centrifuge IVD

MHRA Device ID: 163710•Ref: 163710

Device Type

In Vitro Diagnostic Device

Devices

Cytological centrifuge IVD

Type

Class A

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Name

Sakura Seiki Co., Ltd.

Address

75-5 Imojiya

Chikuma-shi, Nagano, Japan

Created Date

Feb 1, 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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Cytological centrifuge IVD - UK MHRA Medical Device Registration

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