Activated clotting time (ACT) IVD, kit, clotting - UK MHRA Medical Device Registration

Activated clotting time (ACT) IVD, kit, clotting is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 113135. The device is manufactured by Pentapharm AG from Switzerland, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Emergo Consulting (UK) Limited .

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Activated clotting time (ACT) IVD, kit, clotting

MHRA Device ID: 113135•Ref: 113135

Device Type

In Vitro Diagnostic Device

Devices

Activated clotting time (ACT) IVD, kit, clotting

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Oct 30, 2024

Manufacturer Information

Name

Pentapharm AG

Address

Dornacherstrasse 112

Aesch BL, Switzerland

Created Date

Nov 16, 2021

Authorized Representative

Name

Emergo Consulting (UK) Limited

Relationship Type

UK Responsible Person

Address

Compass House, Vision Park Histon c/o Cr360 – UL International

Cambridge, England, United Kingdom

Postcode: CB24 9BZ

DJ Fang

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Activated clotting time (ACT) IVD, kit, clotting - UK MHRA Medical Device Registration

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