CODMAN HAKIM SIPHONGUARD RICKHAM NS5031A

GUDID 10886704046622

CODMAN HAKIM Programmable Valve Micro II Valve, with SIPHONGUARD and Unitized SALMON-RICKHAM Reservoir (Plastic Base) Reservoir arm length 18mm Programmable in steps of 10mm H2O (98 Pa): 30mm H2O to 200mm H2O (294 Pa - 1960 Pa) Includes: Ventricular Catheter 14cm, Stylet, 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 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: 10886704046622
• NIH Device Record Key: 90803068-22e6-4f14-b79c-196e97a40a35
• Commercial Distribution Discontinuation: 2022-09-01
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CODMAN HAKIM SIPHONGUARD RICKHAM
• Version Model Number: NS5031A
• Catalog Number: NS5031A
• 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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• 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)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
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• Phone: +1(800)255-2500
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Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged
• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged
• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged
• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged
• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged
• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged
• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged
• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged
• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged
• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged
• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged
• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged
• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged
• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged
• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged
• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged
• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged
• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged

Device Identifiers

Device Issuing Agency	Device ID
GS1	10381780525080 [Primary]
GS1	10886704046622 [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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• 10886704085386 - CEREGLIDE: 2023-07-17 CEREGLIDE 71 Intermediate Catheter 137 cm 0.071 in (1.80 mm) 0.0820 in (2.08 mm) 0.0825 in (2.10 mm)
• 10886704085409 - CEREGLIDE: 2023-07-17 CEREGLIDE 71 Intermediate Catheter 132 cm 0.071 in (1.80 mm) 0.0820 in (2.08 mm) 0.0825 in (2.10 mm)
• 10886704085423 - CEREGLIDE: 2023-07-17 CEREGLIDE 71 Intermediate Catheter 125 cm 0.071 in (1.80 mm) 0.0820 in (2.08 mm) 0.0825 in (2.10 mm)
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• 10886704015505 - CRANIOPLASTIC: 2022-03-01 Codman CRANIOPLASTIC Resinous Material for Repairing Cranial Defects