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Scannav Anatomy PNB gets FDA approval

Scannav Anatomy PNB gets FDA approval

Scannav Anatomy PNB gets FDA approval

Intelligent Ultrasound, a company that develops software with the aim of improving the quality, reliability and diagnostic power of recently acquired medical ultrasound Again Approval from the US Food and Drug Administration (FDA) for the Scannew Anatomy PNB (Peripheral Nerve Block) device.

Scannav Anatomy PNB is an artificial intelligence (AI) powered medical device and system to be used during field anesthesia procedures. The device is designed to help healthcare professionals perform ultrasound-guided PNB and works by highlighting the live ultrasound image to help identify key anatomical structures when performing peripheral nerve block procedures. Scannew Anatomy PNB is designed to enhance the accuracy of ultrasound imaging through color overlay of key sono-anatomical structures during live ultrasound.

This device can prove to be a game changer for PNB. With an AI assistant that highlights anatomical structures via ultrasound, PNB accuracy and ultimately safety can be greatly improved. ScanNav Anatomy PNB uses AI technology and will provide scan evaluation of anatomical structures in the body by identifying and grading ultrasound images with deep-learning technology.

Scannev Anatomy PNB supports the following nine popular ultrasound-guided regional anesthesia procedures: interscalene, superior trunk, supraclavicular, axillary, erector spina plane, rectus sheath, supraguinal fascia iliaca, adductor canal/sub-sartorial femoral triangle, and popliteal. Additionally, the device is compatible with general-purpose ultrasound machines with an HDMI or DVI second monitor port.

Since the FDA has classified ScanNav Anatomy PNB under Again program, the agency concluded that there are no devices already on the market that meet the clinical need, leading to new common types of real-time anatomy visualization and labeling devices for ultrasound-guided regional anesthesia. of device classification.

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