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News

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Happy anniversary – pfmmedical celebrates 50 years of success

Just before Christmas in 1971, a company called pfm Plastik für die Medizin GmbH came into being. Now called pfm medical ag, it has been growing ever since – while the company still has the same head office in Cologne, it now boasts production facilities and sales outlets at twelve locations in eight countries around the world. Operating on an international scale and yet still family owned, this medium-sized company employs around 660 people and...

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MDR-certified: APL and LL-Sets for the BodyGuard and LimLess® infusion pumps

The pfmmedical group is proud to announce that it has been granted certification under the EU Medical Device Regulation for its product groups APL 2002® Set, infusion tubing sets for use with BodyGuard infusion pumps*, and the LL 2012 Set, infusion tubing for use with the LimLess® infusion pump. These premium quality medical devices, manufactured by pfm medical mepro gmbh, belong to the “Infusion systems and accessories” product group....

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pfmmedical leads the way with MDR compliance

Many companies are facing major challenges in having to comply with the new requirements of the EU Medical Device Regulation, or MDR. But pfm medical ag, a medium-sized, family-owned company based in Germany which operates internationally and has been delivering special solutions in the healthcare sector for 50 years, saw the importance of taking prompt action to adapt to these changes right from the outset. pfmmedical is a medical technology...

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Titanised meshes for breast surgery are now certified according to MDR

Our titanised mesh implants for breast surgery, TiLOOP® Bra Pocket and TiLOOP® Bra have been certified according to MDR (EU) 2017/745 since last week. Both products have successfully passed the certification process. (EU Certificate no. 51334-61). This makes us one of the first mesh implant manufacturers whose Class III products for breast surgery have been successfully certified according to MDR (EU) 2017/745. With this early certification date,...

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Start of the Magnetic Resonance Outcome (MRO) study to evaluate the ClearCoast™ MRI system

The ClearCoast™ MRI system makes it possible to perform precise intraoperative margin evaluation during breast-conserving surgery – often eliminating the need for the patient to undergo a second operation. In the MRO study, launched in June 2021, surgeons are able for the first time to evaluate the tissue margin during the operation. The aim: to reduce the rate of second operations by 80 percent. Being able to evaluate the margin quickly and...

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Services

  • Customer Service
  • Returns
  • Service Gas Sterilisation
  • E-Commerce Services
  • Logistic Services
  • Technical Service and Support
  • Surgery workshops
  • Download center

Application fields

  • Treatment of pelvic organ descent
  • Breast reconstruction
  • Hernia surgery

Knowledge

  • ENFit™- A standard in enteral nutrition
  • Exsiccation prophylactic
  • Pleural effusion and ascites
  • Prevention of Needle and Stick Injuries
  • Studies
  • Electronic study database
  • The human heart and possible defects
  • Titanisation
  • Glossary

Company

  • News
  • About us
  • Our mission, vision and values
  • Facts and Figures
  • Management Board and Supervisory Board
  • Subsidiaries
  • Partners
  • History of pfm medical
  • Research - Development - Production
  • Purchasing
  • Quality Management
  • Compliance
  • Exhibitions, congresses and workshops

Career

  • Working at pfm medical

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