PERGO MEDIKAL VE ILAC SANAYI ANONIM SIRKETI

Pergo Medikal Ve Ilac Sanayi Anonim Şirketi produces reusable and single-use surgical suction system components, such as collection containers, canister liners, and tubing. Their portfolio also includes disposable medical drapes, aspiration trays, and hermetic postsurgical eye shields, as well as single-use suction/irrigation system holders. These devices are designed for use in surgical procedures to manage fluids and maintain sterile environments.

The company is based in the United States, where it operates and manufactures its medical devices. Their location ensures compliance with U.S. regulatory requirements for medical device production and distribution.

Devices produced by Pergo Medikal Ve Ilac Sanayi Anonim Şirketi are listed in the FDA’s Unique Device Identification (UDI) database. This registry helps track and identify medical devices under U.S. regulatory oversight, ensuring transparency and traceability for healthcare providers and regulators.

The company’s devices fall into two primary regulatory classes: Class I and Class II. Class I devices generally pose minimal risk and may require less regulatory scrutiny, while Class II devices involve a higher level of risk and typically require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use, potential risks, and the body part involved.