CODMAN HAKIM RICKHAM SIPHONGUARD NS5061

GUDID 10886704046844

CODMAN HAKIM Programmable Valve Micro II Valve with RICKHAM Reservoir and SIPHONGUARD Device with Unitized Distal Catheter 120cm Programmable in steps of 10mm H2O (98Pa): 30mm H2O to 200mm H2O (294Pa-1960Pa) Includes: 14cm Ventricular Catheter, Stylet, 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: 10886704046844
• NIH Device Record Key: 19ae6440-583f-40c3-8daf-ca572e1bb6c2
• Commercial Distribution Discontinuation: 2022-09-01
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CODMAN HAKIM RICKHAM SIPHONGUARD
• Version Model Number: NS5061
• Catalog Number: NS5061
• Company DUNS: 607846297
• Company Name: CODMAN & SHURTLEFF, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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	10886704046844 [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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