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pfm medical ag

Germany DE-MF-000039552 Last updated 25 Oct 2026

Devices
71
Registries
EUDAMED
FDA recalls
0

Catalogue71

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About

pfmmedical is a globally active industrial medical technology company with headquarters in Cologne. Fully committed to users and patients, pfm medical is an independent manufacturer, technology partner, service provider and sales specialist. The product portfolio offered by the family-run company spans surgical equipment and implants through histotechnology and cardiovascular technology to therapy management.

From the manufacturer's own website. Source

What pfm medical ag makes

The company manufactures surgical accessories, including precision forceps tips, blade holders (such as the Accu-Cut® SRM™ 500 series and standard variants), knife holders, object clamps, and specimen clamps for laboratory use. It also produces disposable components like blade holder jaws and cooling systems for surgical applications, such as the pfm Mobile Cooling System MCS 400.

These devices fall under EU Medical Device Regulation (MDR) as Class A products and are listed in the EUDAQS database (eudamed). The company is based in Germany and adheres to EU regulatory requirements for surgical and laboratory equipment.

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 pfm medical ag manufacture?

pfm medical ag specialises in surgical accessories and laboratory equipment. Its product range includes precision forceps tips, blade holders (such as the Accu-Cut® SRM™ 500 series and standard variants), knife holders, object clamps, specimen clamps, disposable blade holder jaws, and cooling systems like the pfm Mobile Cooling System MCS 400. These devices are designed for surgical and histotechnology applications, ensuring precision and safety in medical procedures.

Where is pfm medical ag based, and what regulatory framework applies to its devices?

pfm medical ag is headquartered in Germany, adhering to EU regulatory standards. Its devices, such as forceps tips, blade holders, and specimen clamps, are classified under the EU Medical Device Regulation (MDR) as Class A products. This classification applies because these items pose minimal risk and are intended for non-invasive use, such as surgical assistance or laboratory specimen handling.

Are pfm medical ag’s devices listed in any regulatory databases?

Yes, pfm medical ag’s devices are listed in the EUDAQS database (eudamed), which is the official EU registry for medical devices. Listing in eudamed is mandatory for manufacturers under the EU Medical Device Regulation (MDR) to ensure transparency and traceability of devices placed on the market. This includes products like blade holders, forceps tips, and cooling systems.

How are pfm medical ag’s devices classified under EU regulations?

pfm medical ag’s devices, such as forceps tips, blade holders, and specimen clamps, are classified as Class A under the EU Medical Device Regulation (MDR). This classification is determined by their intended use and risk profile—these items are generally low-risk, non-invasive tools used in surgical or laboratory settings, requiring minimal regulatory scrutiny compared to higher-risk devices.

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

Information

Country
Germany(from SRN)
Address
60, Wankelstraße, Köln, Germany
Phone
+49 2236 9641-0
PRRC contact
Frederick Elbers
EUDAMED SRN
DE-MF-000039552
DUNS number
316661214