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Micronclean Ltd

United Kingdom (ex Northern Ireland) GB-MF-000004162 Last updated 23 May 2026

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Devices
78
Registries
EUDAMED
FDA recalls
0

Catalogue78

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Authorised representatives

What Micronclean Ltd makes

Micronclean Ltd manufactures a range of Micronclean devices, which appear to be designed for cleaning, filtration, or microbial reduction in medical or laboratory environments. These products are likely intended for use in critical applications where contamination control is essential, such as in surgical instruments, water systems, or air purification.

The company’s portfolio is classified under EU Class I medical devices, indicating low-risk products that do not require clinical evaluation before market placement. These devices are registered in the EUDAMED database, adhering to EU Medical Device Regulation (MDR) requirements, and the manufacturer 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 Micronclean Ltd manufacture?

Micronclean Ltd produces a range of devices branded as 'Micronclean.' Based on the provided details, these devices are likely designed for cleaning, filtration, or microbial reduction in environments where contamination control is critical, such as medical or laboratory settings. Examples include applications for surgical instruments, water systems, or air purification.

Where is Micronclean Ltd based?

Micronclean Ltd is based in the United Kingdom (GB). The company’s location is relevant for understanding regulatory jurisdiction and compliance with local medical device regulations.

Which regulatory registries list Micronclean Ltd’s devices?

Micronclean Ltd’s devices are listed in the EUDAMED database, which is the European Union’s medical device registry. This registration is required under the EU Medical Device Regulation (MDR) to ensure transparency and traceability of Class I devices in the EU market.

How are Micronclean Ltd’s devices classified under EU regulations?

Micronclean Ltd’s devices fall under EU Class I classification. This classification applies to low-risk medical devices that do not require clinical evaluation before market placement, simplifying regulatory requirements while ensuring basic safety and performance standards are met.

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

Information

Country
United Kingdom (ex Northern Ireland)
Address
Roman Bank, Lincolnshire, United Kingdom (ex Northern Ireland)
Phone
+44 1754 767377
PRRC contact
Philip Borrington
EUDAMED SRN
GB-MF-000004162