CODMAN HAKIM RICKHAM SIPHONGUARD NS0598

GUDID 10886704046028

CODMAN HAKIM Precision Fixed Pressure Valve MICRO II With SALMON-RICKHAM Reservoir and SIPHONGUARD Device Operating Pressure: 70mm H2O Plus or Minus 10mm H2O (686 Pa Plus or Minus 98 Pa) Medium Low Range Includes: Ventricular Catheter 14cm, Stylet, Nonunitized Peritoneal Catheter 120cm, Priming Adapter and Information Manual

CODMAN & SHURTLEFF, INC.

Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt Ventriculoperitoneal shunt

• Primary Device ID: 10886704046028
• NIH Device Record Key: 12da4ac6-6250-4513-8a6d-3d452c016682
• Commercial Distribution Discontinuation: 2022-09-01
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CODMAN HAKIM RICKHAM SIPHONGUARD
• Version Model Number: NS0598
• Catalog Number: NS0598
• Company DUNS: 607846297
• Company Name: CODMAN & SHURTLEFF, INC.
• 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)255-2500
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Device Identifiers

Device Issuing Agency	Device ID
GS1	10886704046028 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K091346

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: 2021-10-12
• Device Publish Date: 2015-09-20

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