Integra Flow Regulating Valve Low Flow 909513

GUDID 10381780033851

The Integra Flow Regulating Valves Low Flow (Standard, Mini) are implantable hydrocephalus valve systems for controlled cerebrospinal fluid (CSF) drainage from the ventricles to the peritoneal cavity or other appropriate drainage site such as the heart’s right atrium. Unlike conventional valves, the Integra Flow Regulating Valve Low Flow is a variable resistance valve that maintains drainage at a constant rate, between 8 and 17 ml/hr, within the physiological range of intracranial pressure.

INTEGRA NEUROSCIENCES IMPLANT (FRANCE)

Ventriculo-peritoneal/atrial shunt Ventriculo-peritoneal/atrial shunt Ventriculo-peritoneal/atrial shunt Ventriculo-peritoneal/atrial shunt Ventriculo-peritoneal/atrial shunt Ventriculo-peritoneal/atrial shunt Ventriculo-peritoneal/atrial shunt Ventriculo-peritoneal/atrial shunt Ventriculo-peritoneal/atrial shunt Ventriculo-peritoneal/atrial shunt Ventriculo-peritoneal/atrial shunt Ventriculo-peritoneal/atrial shunt Ventriculo-peritoneal/atrial shunt Ventriculo-peritoneal/atrial shunt Ventriculo-peritoneal/atrial shunt Ventriculo-peritoneal/atrial shunt Ventriculo-peritoneal/atrial shunt Ventriculo-peritoneal/atrial shunt Ventriculo-peritoneal/atrial shunt

• Primary Device ID: 10381780033851
• NIH Device Record Key: f8abc4b1-7d68-4072-82b7-81f76760ae04
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Integra Flow Regulating Valve Low Flow
• Version Model Number: 909513
• Catalog Number: 909513
• Company DUNS: 531408342
• Company Name: INTEGRA NEUROSCIENCES IMPLANT (FRANCE)
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room temperature

Device Identifiers

Device Issuing Agency	Device ID
GS1	10381780033851 [Primary]
HIBCC	M2729095131 [Secondary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K042192

FDA Product Code

• JXG: Shunt, central nervous system and components

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2021-04-07
• Device Publish Date: 2015-10-01

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