For connecting Double Pump RF or Double Pump to Arthrex APS II, Atlantech Revolu
For connecting Double Pump RF or Double Pump to Arthrex APS II, Atlantech Revolution, FMS Duo+
For connecting Double Pump RF or Double Pump to BSM PowerTek II Plus, Stryker TP
For connecting Double Pump RF or Double Pump to BSM PowerTek II Plus, Stryker TPS, Stryker Core
For connecting Double Pump RF or Double Pump to ConMed-Linvatec Advantage D 3000
For connecting Double Pump RF or Double Pump to ConMed-Linvatec Advantage D 3000; red shaver port
The Insightra Medical Freedom Inguinal Hernia Implant (ProFlor™) is a sterile, p
The Insightra Medical Freedom Inguinal Hernia Implant (ProFlor™) is a sterile, polypropylene implant device designed for use in the open repair of inguinal hernias. A delivery device, sold separately, is used to deploy the implant into the prepared hernia defect site.
The Insightra Medical Freedom Inguinal Hernia Implant (ProFlor™) is a sterile, p
The Insightra Medical Freedom Inguinal Hernia Implant (ProFlor™) is a sterile, polypropylene implant device designed for use in the open repair of inguinal hernias. A delivery device, sold separately, is used to deploy the implant into the prepared hernia defect site.
The Insightra Medical Freedom Inguinal Hernia Implant (ProFlor™) is a sterile, p
The Insightra Medical Freedom Inguinal Hernia Implant (ProFlor™) is a sterile, polypropylene implant device designed for use in the open repair of inguinal hernias. A delivery device, sold separately, is used to deploy the implant into the prepared hernia defect site.
The Insightra Intra Aortic Balloon Catheter Kit is used in conjunction with an i
The Insightra Intra Aortic Balloon Catheter Kit is used in conjunction with an intra-aortic balloon pumping circuit for the emergency treatment of patients in cardiogenic shock. This condition occurs in patients post acute myocardial infarction, or with reduced cardiac output post open-heart surgery.
The Insightra Intra Aortic Balloon Catheter Kit is used in conjunction with an i
The Insightra Intra Aortic Balloon Catheter Kit is used in conjunction with an intra-aortic balloon pumping circuit for the emergency treatment of patients in cardiogenic shock. This condition occurs in patients post acute myocardial infarction, or with reduced cardiac output post open-heart surgery.
The Insightra Intra Aortic Balloon Catheter Kit is used in conjunction with an i
The Insightra Intra Aortic Balloon Catheter Kit is used in conjunction with an intra-aortic balloon pumping circuit for the emergency treatment of patients in cardiogenic shock. This condition occurs in patients post acute myocardial infarction, or with reduced cardiac output post open-heart surgery.
The Modulare System is used to secure various types of catheters to the patient’
The Modulare System is used to secure various types of catheters to the patient’s skin. The device uses a post and securement cover to attach itself to either the suture tab of the catheter or mating hole on Modulare accessories. An adhesive base secures the Modulare system to the patient to allow for safe and secure placement of the catheter onto the patient. The Modulare system is disposable and designed to be placed on the patient for a time to not to exceed 7 days.
The Modulare System is used to secure various types of catheters to the patient’
The Modulare System is used to secure various types of catheters to the patient’s skin. The device uses a post and securement cover to attach itself to either the suture tab of the catheter or mating hole on Modulare accessories. An adhesive base secures the Modulare system to the patient to allow for safe and secure placement of the catheter onto the patient. The Modulare system is disposable and designed to be placed on the patient for a time to not to exceed 7 days.
The Freedom™ Ventral Hernia Repair System consists of a synthetic and permanent
The Freedom™ Ventral Hernia Repair System consists of a synthetic and permanent polypropylene Octomesh™ implant and a disposable strap passer. The implant has a central body with 8 radiating straps. The straps pass through the abdominal wall, leaving them lying in tissue tunnels created by the passer. The straps hold the body of the mesh in place.
OXJ
Mesh, Surgical, Non-Absorbable, Large Abdominal Wall Defects
The Freedom™ Ventral Hernia Repair System consists of a synthetic and permanent
The Freedom™ Ventral Hernia Repair System consists of a synthetic and permanent polypropylene Octomesh™ implant and a disposable strap passer. The implant has a central body with 8 radiating straps. The straps pass through the abdominal wall, leaving them lying in tissue tunnels created by the passer. The straps hold the body of the mesh in place.
OXJ
Mesh, Surgical, Non-Absorbable, Large Abdominal Wall Defects
The Freedom™ Ventral Hernia Repair System consists of a synthetic and permanent
The Freedom™ Ventral Hernia Repair System consists of a synthetic and permanent polypropylene Octomesh™ implant and a disposable strap passer. The implant has a central body with 8 radiating straps. The straps pass through the abdominal wall, leaving them lying in tissue tunnels created by the passer. The straps hold the body of the mesh in place.
OXJ
Mesh, Surgical, Non-Absorbable, Large Abdominal Wall Defects
The Freedom™ Ventral Hernia Repair System consists of a synthetic and permanent
The Freedom™ Ventral Hernia Repair System consists of a synthetic and permanent polypropylene Octomesh™ implant and a disposable strap passer. The implant has a central body with 8 radiating straps. The straps pass through the abdominal wall, leaving them lying in tissue tunnels created by the passer. The straps hold the body of the mesh in place.
OXJ
Mesh, Surgical, Non-Absorbable, Large Abdominal Wall Defects
The Freedom™ Ventral Hernia Repair System consists of a synthetic and permanent
The Freedom™ Ventral Hernia Repair System consists of a synthetic and permanent polypropylene Octomesh™ implant and a disposable strap passer. The implant has a central body with 8 radiating straps. The straps pass through the abdominal wall and hold the body of the mesh in place.
OXJ
Mesh, Surgical, Non-Absorbable, Large Abdominal Wall Defects
The Insightra Medical Freedom Inguinal Hernia Implant (ProFlor™) is a sterile, p
The Insightra Medical Freedom Inguinal Hernia Implant (ProFlor™) is a sterile, polypropylene implant device designed for use in the open repair of inguinal hernias. A delivery device is used to deploy the implant into the prepared hernia defect site.
The Insightra Medical Freedom Inguinal Hernia Implant (ProFlor™) is a sterile, p
The Insightra Medical Freedom Inguinal Hernia Implant (ProFlor™) is a sterile, polypropylene implant device designed for use in the open repair of inguinal hernias. A delivery device is used to deploy the implant into the prepared hernia defect site.
The Insightra Medical Freedom Inguinal Hernia Implant (ProFlor™) is a sterile, p
The Insightra Medical Freedom Inguinal Hernia Implant (ProFlor™) is a sterile, polypropylene implant device designed for use in the open repair of inguinal hernias. A delivery device is used to deploy the implant into the prepared hernia defect site.
The Insightra Medical Freedom Inguinal Hernia Implant (ProFlor™) is a sterile po
The Insightra Medical Freedom Inguinal Hernia Implant (ProFlor™) is a sterile polypropylene implant device designed for use in the open repair of inguinal hernias. A delivery device is used to deploy the implant into the prepared hernia defect site.
The Insightra Medical Freedom Inguinal Hernia Implant (ProFlor™) is a sterile, p
The Insightra Medical Freedom Inguinal Hernia Implant (ProFlor™) is a sterile, polypropylene implant device designed for use in the open repair of inguinal hernias. A delivery device is used to deploy the implant into the prepared hernia defect site.
The Insightra Medical Freedom Inguinal Hernia Implant (ProFlor™) is a sterile, p
The Insightra Medical Freedom Inguinal Hernia Implant (ProFlor™) is a sterile, polypropylene implant device designed for use in the open repair of inguinal hernias. A delivery device is used to deploy the implant into the prepared hernia defect site.
For temporary bridging of fascial defects where primary closure is not possible,
For temporary bridging of fascial defects where primary closure is not possible, including but not limited to, abdominal compartment syndrome.
For temporary bridging of abdominal wall openings where primary closure is not p
For temporary bridging of abdominal wall openings where primary closure is not possible and/or repeat abdominal entries are necessary.
Bioresorbable protective sheet made from polylactide: a copolymer of 70:30 Poly(
Bioresorbable protective sheet made from polylactide: a copolymer of 70:30 Poly(L-lactide-co-D,L-lactide). To be used for management and protection of tendon injuries in which there has been no substantial loss of tendon tissue. Minimizes tissue attachment to the device in case of direct contact with the tissues. Also indicated for reinforcement of soft tissues repaired by suture or suture anchors, during tendon repair surgery. Reinforces soft tissue and provides a remodelable scaffold that is replaced by the patient’s own soft tissue. The device is indicated for open and laparoscopic/endoscopic procedures.
Bioresorbable protective sheet made from polylactide: a copolymer of 70:30 Poly(
Bioresorbable protective sheet made from polylactide: a copolymer of 70:30 Poly(L-lactide-co-D,L-lactide). To be used for management and protection of tendon injuries in which there has been no substantial loss of tendon tissue. Minimizes tissue attachment to the device in case of direct contact with the tissues. Also indicated for reinforcement of soft tissues repaired by suture or suture anchors, during tendon repair surgery. Reinforces soft tissue and provides a remodelable scaffold that is replaced by the patient’s own soft tissue. The device is indicated for open and laparoscopic/endoscopic procedures.
Bioresorbable protective sheet made from polylactide: a copolymer of 70:30 Poly(
Bioresorbable protective sheet made from polylactide: a copolymer of 70:30 Poly(L-lactide-co-D,L-lactide). To be used wherever temporary wound support is required, to reinforce soft tissues where weakness exists in the urological, gynecological or gastroenterological anatomy or for the repair of hernia or other fascial defects that require the addition of a reinforcing or bridging material to obtain the desired surgical result. Minimizes tissue attachments to the device in case of direct contact with the viscera. Indicated for open and laparoscopic procedures.
Bioresorbable protective sheet made from polylactide: a copolymer of 70:30 Poly(
Bioresorbable protective sheet made from polylactide: a copolymer of 70:30 Poly(L-lactide-co-D,L-lactide). To be used wherever temporary wound support is required, to reinforce soft tissues where weakness exists in the urological, gynecological or gastroenterological anatomy or for the repair of hernia or other fascial defects that require the addition of a reinforcing or bridging material to obtain the desired surgical result. Minimizes tissue attachments to the device in case of direct contact with the viscera. Indicated for open and laparoscopic procedures.
Bioresorbable protective sheet made from polylactide: a copolymer of 70:30 Poly(
Bioresorbable protective sheet made from polylactide: a copolymer of 70:30 Poly(L-lactide-co-D,L-lactide). To be used wherever temporary wound support is required, to reinforce soft tissues where weakness exists in the urological, gynecological or gastroenterological anatomy or for the repair of hernia or other fascial defects that require the addition of a reinforcing or bridging material to obtain the desired surgical result. Minimizes tissue attachments to the device in case of direct contact with the viscera. Indicated for open and laparoscopic procedures.
Bioresorbable protective sheet made from polylactide: a copolymer of 70:30 Poly(
Bioresorbable protective sheet made from polylactide: a copolymer of 70:30 Poly(L-lactide-co-D,L-lactide). To be used wherever temporary wound support is required, to reinforce soft tissues where weakness exists in the urological, gynecological or gastroenterological anatomy or for the repair of hernia or other fascial defects that require the addition of a reinforcing or bridging material to obtain the desired surgical result. Minimizes tissue attachments to the device in case of direct contact with the viscera. Indicated for open and laparoscopic procedures.