United Kingdom MHRA device registration 113134

Activated clotting time (ACT) IVD, control

United Kingdom·In Vitro Diagnostic Device·Pentapharm AG·Registered Nov 26, 2024

Registration details

Device ID: 113134
MHRA Reference Number: 113134
Date Registered: Nov 26, 2024
Last Updated: Oct 30, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Activated clotting time (ACT) IVD, control
Type: IVD General

Manufacturer

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

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Other products from Pentapharm AG

Additional devices registered by the same manufacturer

Activated protein C resistance ratio (APCR) IVD, controlNov 26, 2024

Type: In Vitro Diagnostic Device

Device ID: 113132

Reptilase time IVD, kit, clottingNov 26, 2024

Type: In Vitro Diagnostic Device

Device ID: 113131

Activated clotting time (ACT) IVD, kit, clottingNov 26, 2024

Type: In Vitro Diagnostic Device

Device ID: 113135

Activated protein C resistance ratio (APCR) IVD, kit, clottingNov 26, 2024

Type: In Vitro Diagnostic Device

Device ID: 113133

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About this record

Activated clotting time (ACT) IVD, control is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 113134. 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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