6 results
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11ms
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Sources: EU EUDAMED, US FDA
Cordis OPTEASE Retrieval Inferior Vena Cava (IVC) Filter***REF Cat. No.***466F220A and 466F220B***Vena Cava Filter and Introduction Kit***(BRITE TIP Catheter Sheath Introducer and Angiographic Vessel Dilator)***Cordis***a Johnson and Johnson Company***ENDOVASCULAR*** Label No. SB 10247519.2/***LB466F220AO.5***omoraoro/2012.050794***Do not resterilize***. Product Usage: The OPTEASE Vena Cava Filter is indicated for use in the prevention of recurrent pulmonary embolism (PE) via percutaneous placement in the vena cava in several situations: Pulmonary thromboembolism when anticoagulants are contraindicated; Failure of anticoagulant therapy for thromboembolic disease; Emergency treatment following massive pulmonary embolism where anticipated benefits of conventional therapy are reduced and Chronic, recurrent pulmonary embolism where anticoagulant therapy has failed, or is contraindicated.
FDA Enforcement
Class I
·Terminated·Cordis Corporation·August 14, 2013
Cordis SUPER TORQUE MB 5F PIG, Angiographic Catheter, REF 532-598C
FDA Enforcement
Class I
·Terminated·Cordis Corporation·September 22, 2021
Cordis SUPER TORQUE MB 5F PIG, Angiographic Catheter, REF 532-598A
FDA Enforcement
Class I
·Terminated·Cordis Corporation·September 22, 2021
Cordis SUPER TORQUE MB 5F PIG, Angiographic Catheter, REF 532-598B
FDA Enforcement
Class I
·Terminated·Cordis Corporation·September 22, 2021
Cordis 5F UNIVERSAL FLUSH F4 SUPER TORQUE MB, SPECIAL, Angiographic Catheter, REF SRD6785MB
FDA Enforcement
Class I
·Terminated·Cordis Corporation·September 22, 2021
Cordis 5F SUPER TORQUE PIG PIGTAIL SPECIAL, Angiographic Catheter, REF SRD7040MB
FDA Enforcement
Class I
·Terminated·Cordis Corporation·September 22, 2021