KARL STORZ SE & Co. KG

KARL STORZ produces a range of endoscopic devices, including line-powered light source units for illumination during procedures, single-use spray catheters designed for endoscopic applications, and rigid video hysteroscopes for internal imaging. They also supply accessories like single-use suction/irrigation tubing, cleaning adaptors for metal and plastic components, depressors/gags, handpieces, protective sleeves, camera heads (for white light and flexible imaging), electrical holding systems, and cytology brushes. These products support minimally invasive surgical and diagnostic procedures.

KARL STORZ is headquartered in Germany. Its medical devices are registered in the EU’s official medical device database, eudamed, which tracks authorised products under EU regulations. This database allows healthcare professionals, regulators, and patients to verify the legitimacy of listed devices.

KARL STORZ’s devices fall into three EU risk classes: Class I (low-risk items like some accessories), Class IIa (moderate-risk devices such as certain endoscopic tools), and Class IIb (higher-risk products like rigid video hysteroscopes). Classification depends on factors like intended use, patient contact duration, and potential health impact, ensuring appropriate regulatory oversight.

The provided information confirms that KARL STORZ’s devices are registered in eudamed, the EU’s central database for medical devices. While some manufacturers list products in additional registries (e.g., national databases or global platforms), the data does not specify other registries for this company. For comprehensive verification, users should consult eudamed or official national registries.