Integra DP™ Valve
Limits uncertainty ensuring pressure control and resistance to occlusion.
The original ball-in-cone and spring mechanism of the Integra DP™ Valve System has been used for over 30 years in the treatment of hydrocephalus.
Five color-coded pressure ranges are offered in standard and pediatric versions, and a wide variety of configuration options are available to accommodate surgeon preference.
Integra DP valve systems are implantable devices which serve as a parallel flow pathway to divert cerebrospinal fluid (CSF) from the cerebral ventricles to an appropriate drainage site. They provide controlled intraventricular pressure and CSF drainage in patients with hydrocephalus or other conditions in which CSF flow and/or absorption is impaired. The very low pressure valve (blue band) is used for postoperative drainage of hygromas and other extraventricular conditions.
Integra hydrocephalus valve systems and components should not be used when an infection exists along the shunt pathway (meningitis, ventriculitis, peritonitis). Postponement of shunt or component implantation is advisable if infection is present anywhere in the body (septicemia or bacteremia). The use of the ventriculoatrial approach is contraindicated in patients with serious heart or cardiopulmonary disease.
INTEGRA DP VALVES
|901112||Integra DP™ Standard Valve System, Finned Catheter, Very Low Pressure|
|901113||Integra DP™ Standard Valve Unit, Very Low Pressure|
|901122||Integra DP™ Standard Valve System, Finned Catheter, Low Pressure|
|901123||Integra DP™ Standard Valve Unit, Low Pressure|
|901125||Integra DP™ Standard Valve System, Straight Catheter, Low Pressure|
|901142||Integra DP™ Standard Valve System, Finned Catheter, Medium Pressure|
|901143||Integra DP™ Standard Valve Unit, Medium Pressure|
|901145||Integra DP™ Standard Valve System, Straight Catheter, Medium Pressure|
|901162||Integra DP™ Standard Valve System, Finned Catheter, High Pressure|
|901163||Integra DP™ Standard Valve Unit, High Pressure|
|901165||Integra DP™ Standard Valve System, Straight Catheter, High Pressure|
|901182||Integra DP™ Standard Valve System, Finned Catheter, Very High Pressure|
|901183||Integra DP™ Standard Valve Unit, Very High Pressure|
PED INTEGRA DP VALVES
|902012||Integra DP™ Pediatric Valve System, Finned Catheter, Very Low Pressure|
|902045||Integra DP™ Pediatric Valve System, Finned Catheter, Low Pressure|
|902080||Integra DP™ Pediatric Valve System, Finned Catheter, Medium Pressure|
|902123||Integra DP™ Pediatric Valve Unit, Low Pressure|
|902125||Integra DP™ Pediatric Valve System, Finned Catheter, High Pressure|
|902143||Integra DP™ Pediatric Valve Unit, Medium Pressure|
|902163||Integra DP™ Pediatric Valve Unit, High Pressure|
|902525||Integra DP™ Pediatric Valve System, Straight Catheter, High Pressure|
|902545||Integra DP™ Pediatric Valve System, Straight Catheter, Low Pressure|
|902580||Integra DP™ Pediatric Valve System, Straight Catheter, Medium Pressure|
|907122||Integra DP™ Standard Burr Hole System, Low Pressure|
|907142||Integra DP™ Standard Burr Hole System, Medium Pressure|
|907162||Integra DP™ Standard Burr Hole System, High Pressure|
|908112||Integra DP™ Pediatric Burr Hole System, Very Low Pressure|
|908122||Integra DP™ Pediatric Burr Hole System, Low Pressure|
|908142||Integra DP™ Pediatric Burr Hole System, Medium Pressure|
|908162||Integra DP™ Pediatric Burr Hole System, High Pressure|
Regulatory and Legal Information
Class III Medical Devices.
Integra NeuroSciences Implants (France) S.A.S.
2905 route des dolines
06921 Sophia Antipolis Cedex • FRANCE
No EC REP
Availability of these products might vary from a given country or region to another, as a result of speciﬁc local regulatory approval or clearance requirements for sale in such country or region.
• Consult product labels and inserts for any indications, contraindications, hazards, warnings, precautions and instructions for use.
• Non contractual document. Integra reserves the right, without prior notice, to modify the products in order to improve their quality.
• WARNING: Applicable laws restrict these products to sale by or on the order of a physician. All text and diagrams on this page are intended as guidelines and are for illustrative purposes only. No information included on this page is intended to replace the Directions for Use packaged with each Integra product.
Products mentioned in this document are CE class III devices.
Please contact Integra customer service should you need any additional information on devices classification, technical and additional clinical information. All the references numbers mentioned on this document are CE marked according to European council directive 93/42/EEC on Medical Devices, and its relatives, unless specifically identified as “NOT CE MARKED.”
INTEGRA DP is a trademark of Integra LifeSciences Corporation or its subsidiaries. Integra and the Integra logo are registered trademarks of Integra Lifesciences Corporation in the United States and/or other countries.
© 2016 Integra LifeSciences Corporation. All rights reserved. Last revision date: 10/2016.0531216-1-EN
Document for use in Europe, Middle-East & Africa only
For complete product information, please see the Instructions for Use accompanying each product.