Centrifuge tube IVD - UK MHRA Medical Device Registration

Centrifuge tube IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 166415. The device is manufactured by STEMCELL Technologies Canada Inc. from Canada, classified as In Vitro Diagnostic Device. The authorized representative in the UK is MDSS-UK RP LIMITED.

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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Centrifuge tube IVD

MHRA Device ID: 166415•Ref: 166415

Device Type

In Vitro Diagnostic Device

Devices

Centrifuge tube IVD

Type

Class A

Date Registered

Nov 26, 2024

Last Updated

Oct 10, 2024

Manufacturer Information

Name

STEMCELL Technologies Canada Inc.

Address

1618 Station St.

Vancouver, BC, Canada

Created Date

Dec 23, 2021

Authorized Representative

Name

MDSS-UK RP LIMITED

Relationship Type

UK Responsible Person

Address

6 Wilmslow Road, Rusholme

Manchester, England, United Kingdom

Postcode: M14 5TP

DJ Fang

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Other Products from STEMCELL Technologies Canada Inc. (3)

Other Products from Same Authorized Representative (10)

Centrifuge tube IVD - UK MHRA Medical Device Registration

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Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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