Integra® NL8508601

GUDID 10381780537519

Integra® External Drainage System

Integra Lifesciences Corporation

Ventricular cerebrospinal fluid drainage catheterization kit

• Primary Device ID: 10381780537519
• NIH Device Record Key: 2b2eaaaa-e361-4db9-a029-6c5efe14e45e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Integra®
• Version Model Number: NL8508601
• Catalog Number: NL8508601
• Company DUNS: 083171244
• Company Name: Integra Lifesciences Corporation
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	10381780071709 [Previous]
GS1	10381780537519 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K972994

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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-07-08
• Device Publish Date: 2024-06-28

On-Brand Devices [Integra®]

• 10381780072522: 3 FRENCH T-TUBE The Integra Edwards-Barbaro Syringo-Peritoneal Shunt is designed to provide cont
• 10381780024460: 5 FRENCH T-TUBE The Integra Edwards-Barbaro Syringo-Peritoneal Shunt is designed to provide cont
• M248440C10121: Right Horseshoe Gel Pad and Base Assembly
• M248440C10111: Left Horseshoe Gel Pad and Base Assembly
• 10381780344766: Integra® 16.5" BRS RETRACTOR ARM
• 10381780252498: Integra® Hardware Kit for UCHR
• 10381780537519: Integra® External Drainage System
• 10381780537502: Integra® External Drainage System