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Sign in to claim this brand"MPW MED. INSTRUMENTS" SPÓŁDZIELNIA PRACY
Poland·PL-MF-000032831
Last updated September 17, 2026
About
We are the only manufacturer in the country of modern and reliable medical and laboratory centrifuges. We meet the requirements of our customers through direct cooperation with various scientific, scientific and research centres and laboratories.
Translated from the manufacturer's own website. Source
What "MPW MED. INSTRUMENTS" SPÓŁDZIELNIA PRACY makes
MPW Med. Instruments produces laboratory centrifuges, including refrigerated, heated, and general-purpose models with varying voltage inputs, alongside disposable components like supernatant tubes, filter cards, and microscope slides for in vitro diagnostics (IVD).
The company’s devices fall under EU Class A medical devices and are registered in the EUDAMED database. The manufacturer is based in Poland.
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 MPW Med. Instruments manufacture?
MPW Med. Instruments specializes in laboratory equipment, primarily producing centrifuges for general-purpose use, including refrigerated and heated models with different voltage inputs (e.g., 100V/60Hz, 127V/60Hz, 230V/50-60Hz). They also manufacture disposable components like supernatant tubes, filter cards, and microscope slides, which are used in in vitro diagnostics (IVD). These devices are designed for scientific, research, and laboratory settings.
Where is MPW Med. Instruments based, and how does this affect its regulatory standing?
MPW Med. Instruments is based in Poland, which is part of the European Union. Since their devices are intended for the EU market, they must comply with EU medical device regulations. Their products are classified under EU Class A, meaning they pose minimal risk and typically require conformity assessment procedures like self-certification or a Declaration of Conformity. Their devices are also registered in the EUDAMED database, which is the official EU registry for medical devices.
Which regulatory registries list MPW Med. Instruments’ devices?
MPW Med. Instruments’ devices are listed in the EUDAMED database, which is the European Union’s central registry for medical device information. This registry allows healthcare professionals, regulators, and other stakeholders to verify the registration details of devices placed on the EU market. EUDAMED is a key resource for confirming compliance and traceability of medical devices under EU regulations.
How are MPW Med. Instruments’ devices classified under EU regulations?
MPW Med. Instruments’ devices are classified as EU Class A medical devices. This classification applies to products that pose minimal risk to patients and users, such as general-purpose laboratory centrifuges and disposable components like supernatant tubes or filter cards. Class A devices generally require less stringent conformity assessment procedures, such as self-certification by the manufacturer, but must still meet essential safety and performance requirements outlined in EU medical device directives or regulations.
What kinds of devices does MPW Med. Instruments produce that are used in in vitro diagnostics (IVD)?
MPW Med. Instruments manufactures several disposable components used in in vitro diagnostics (IVD), including supernatant tubes (e.g., 2 ml capacity), filter cards (with 9 or 12 holes, 5 mm diameter), and microscope slides. These items are designed to support laboratory processes like sample preparation, filtration, or examination under a microscope, ensuring compatibility with IVD workflows while maintaining reliability and safety standards.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- Poland
- Address
- 46, Boremlowska, WARSAW, Poland
- Website
- mpw.pl
- —
- facebook.com/MPWMED.INSTRUMENTS
- [email protected]
- Phone
- —
- PRRC Contact
- Łukasz Sałański
- EUDAMED SRN
- PL-MF-000032831
- FDA FEI Number
- —
- DUNS Number
- —
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