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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

PRECISE PRO RX CAROTID STENT implant system, Product Codes: PC0520RXC, PC0530RXC, PC0540RXC, PC0620RXC, PC0630RXC, PC0640RXC, PC0720RXC, PC0730RXC, PC0740RXC, PC0820RXC, PC0830RXC, PC0840RXC, PC0920RXC, PC0930RXC, PC0940RXC, PC1030RXC, PC1040RXC

FDA Enforcement
Class I ·Completed·Cordis Corporation·March 24, 2021

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