Bard Denali Inferior Vena Cava Filter Fracture and Embolization
Denali Ivc Filter Mri Safety. New BARD DL900F Denali Vena Cava Filter Femoral 8.4F I.D. 55cm (x The Denali® Vena Cava Filter was determined to be MR-conditional according to the terminology specified in the American Society for Testing and Materials (ASTM) International, Designation: F2503-05 Standard Practice for Marking Medical Devices and Other Items for Safety in the Magnetic Resonance Environment
Bard DENALI Inferior Vena Cava Filter Another “Arm” Fracture Journal from www.jvir.org
Please consult Instructions for Use for product indications for use, contraindications, warnings, precautions, complications, adverse events and detailed safety information. MRI Safety Status: MR Conditional: Human Cell/Tissue Product: false: Device Kit: false: Device Combination Product: false: Single Use: true: Lot Batch: true: Serial Number:
Bard DENALI Inferior Vena Cava Filter Another “Arm” Fracture Journal
The Denali™ Vena Cava Filter should not be retrieved if significant thrombus is in or near the filter The spontaneous migration rate of properly implanted modern IVC filters is approximately 1% However, in vitro testing has demonstrated that nickel is released from this device.
Evaluation of a Device Combining an Inferior Vena Cava Filter and a. Please consult Instructions for Use for product indications for use, contraindications, warnings, precautions, complications, adverse events and detailed safety information. Prior to deployment, verify the location of the filter within the sheath using fluoroscopy and confirm that the filter snare hook is 1cm below the lowest renal or is in the intended location in the inferior vena cava
Retrievable IVC filter deployment, Denali (Bard), Rt femoral approach. *Analysis of the Final DENALI Trial Data: A Prospective, Multicenter Study of the Denali Inferior Vena Cava Filter Standard Practice for Marking Medical Devices and Other Items for Safety in the Magnetic Resonance Environment.