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MicroBioSensor Ltd

United Kingdom (ex Northern Ireland)·GB-MF-000021594

Last updated May 23, 2026

What MicroBioSensor Ltd makes

MicroBioSensor Ltd manufactures the QuickCheck Cassette, a diagnostic test designed for rapid in vitro detection of specific microbial pathogens. This device is intended for point-of-care or near-patient testing to provide immediate results in clinical settings.

The QuickCheck Cassette is classified under IVD General and is registered in the EU’s eudamed database. The company is based in the United Kingdom.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does MicroBioSensor Ltd manufacture?

MicroBioSensor Ltd specialises in in vitro diagnostic (IVD) devices. Specifically, they produce the QuickCheck Cassette, a rapid diagnostic test designed for detecting microbial pathogens in clinical settings. This device is intended for point-of-care or near-patient use, enabling immediate test results.

Where is MicroBioSensor Ltd based, and what is its primary focus?

MicroBioSensor Ltd is based in the United Kingdom. The company focuses on developing and manufacturing diagnostic tools, particularly the QuickCheck Cassette, which falls under the in vitro diagnostic category. This device is designed for quick and reliable detection of microbial pathogens in clinical environments.

Which regulatory registries list MicroBioSensor Ltd’s devices?

MicroBioSensor Ltd’s devices, such as the QuickCheck Cassette, are listed in the EU’s eudamed database. This registry is used to track and provide transparency on in vitro diagnostic medical devices authorised for use within the European Union.

How are MicroBioSensor Ltd’s devices classified?

MicroBioSensor Ltd’s QuickCheck Cassette is classified under the IVD General category. This classification applies to in vitro diagnostic devices that do not pose significant risks and are typically used for routine testing, such as pathogen detection in clinical settings.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
United Kingdom (ex Northern Ireland)
Address
48, Grafton Street, Manchester , United Kingdom (ex Northern Ireland)
LinkedIn
—
Facebook
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Phone
+44 (0)161 606 7401
PRRC Contact
Katie Menchi
EUDAMED SRN
GB-MF-000021594
FDA FEI Number
—
DUNS Number
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Catalogue (1)

DeviceModel / ReferenceRegistriesClassStatus
QuickCheck Cassette MBSQCC100
EUDAMED
IVD GeneralActive

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