Navigated through the sheath-cryobiopsy with the flexible single-use 1.1 mm cryoprobe скачать в хорошем качестве

Navigated through the sheath-cryobiopsy with the flexible single-use 1.1 mm cryoprobe

With the spread of low-dose CT-screening programs for lung cancer, the demand evolves for accurate sampling of detected peripheral pulmonary lesions (PPLs). In this video Prof. Christopher Lambers from Ordensklinikum Linz, Austria demonstrates a peripheral cryobiopsy of a cancerous lesion using the flexible single use 1.1 mm cryoprobe along with an electromagnetic navigation bronchoscopy. Prof. Lambers demonstrates through the sheath croybiopsy after the position of the navigation catheter has been corrected with tomosynthesis. The procedure is described in detailed steps. More information on https://bronchoscopy.erbe-med.com Important note The information, recommendations and other details contained in this medium (“information″) reflect our state of knowledge and the state of the art in science and technology at the time the medium was created. The information is of a general nature, non-binding and intended solely for general information purposes; it does not constitute instructions for use. The information and recommendations contained in this medium do not create any legal obligations on the part of Erbe Elektromedizin GmbH and its affiliated companies (“Erbe″) or any other claims against Erbe. The information does not constitute any guarantees or other information on the nature of the product; such information requires an express contractual agreement with Erbe in each individual case. Erbe is not liable for any kind of damage resulting from following the information on this medium, regardless of any legal grounds for liability. Every user of an Erbe product is responsible for testing the respective Erbe product in advance with regard to its properties and its suitability for the intended type of use or purpose. Suitable type of use of the respective Erbe product can be found in the instructions for use for the respective Erbe product. The user is obliged to ascertain whether the instructions for use available to him/her correspond to the current status of the specific Erbe product. Devices may only be used in accordance with the instructions for use. Information on settings, application sites, application duration and use of the respective Erbe product is based on the clinical experience of individual centers, physicians and clinical literature independent of Erbe as well as post market surveillance and empirical evidence. They constitute reference values, or Experienced Starting Settings, which must be checked by the user to ensure that they are suitable for the specifically planned application. Depending on the circumstances of a specific application, it may be necessary to deviate from the information provided. The user is responsible for checking this when using Erbe products. We wish to note that science and technology are subject to constant development as a result of research and clinical experience. Similarly, medicine and clinical application are constantly evolving as a result of research and technological development. This may also make it necessary for the user to deviate from the information provided on this medium. This medium contains information about Erbe products that may not be approved/cleared in certain countries. The user of the respective Erbe product is obliged to inform himself/herself as to whether the Erbe product he/she is using is legally approved/cleared in his/her country and/or to what extent, if any, there are legal requirements for or restrictions on its use.