CODMAN HAKIM 823284

GUDID 10886704041696

CODMAN HAKIM Precision Fixed Pressure Valve Right Angle Valve and Unitized Distal Catheter Operating Pressure: 100mm H2O Plus or Minus 10mm H2O (980 Pa Plus or Minus 98 Pa) Medium High Range Includes: Precision Valve, 14cm Ventricular Catheter, 120cm Unitized Peritoneal Catheter, Information Manual and Priming Adapter

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 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: 10886704041696
• NIH Device Record Key: 73c6a80b-cebe-4881-bc2a-b5bdc25aa26d
• Commercial Distribution Discontinuation: 2022-09-01
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CODMAN HAKIM
• Version Model Number: 82-3284
• Catalog Number: 823284
• 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

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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
• 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
• 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	10381780519478 [Primary]
GS1	10886704041696 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K944222

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: 3
• Public Version Date: 2021-10-12
• Device Publish Date: 2015-09-20

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