CODMAN IP40812

GUDID 10886704044093

MODEL 400 REFILL TUBING SET

Cerenovus, Inc.

Implantable intrathecal infusion pump, nonprogrammable Implantable intrathecal infusion pump, nonprogrammable Implantable intrathecal infusion pump, nonprogrammable Implantable intrathecal infusion pump, nonprogrammable Implantable intrathecal infusion pump, nonprogrammable Implantable intrathecal infusion pump, nonprogrammable Implantable intrathecal infusion pump, nonprogrammable Implantable intrathecal infusion pump, nonprogrammable Implantable intrathecal infusion pump, nonprogrammable Implantable intrathecal infusion pump, nonprogrammable Implantable intrathecal infusion pump, nonprogrammable Implantable intrathecal infusion pump, nonprogrammable Implantable intrathecal infusion pump, nonprogrammable Implantable intrathecal infusion pump, nonprogrammable Implantable intrathecal infusion pump, nonprogrammable Implantable intrathecal infusion pump, nonprogrammable Implantable intrathecal infusion pump, nonprogrammable Implantable intrathecal infusion pump, nonprogrammable Implantable intrathecal infusion pump, nonprogrammable Implantable intrathecal infusion pump, nonprogrammable Implantable intrathecal infusion pump, nonprogrammable Implantable intrathecal infusion pump, nonprogrammable Implantable intrathecal infusion pump, nonprogrammable Implantable intrathecal infusion pump, nonprogrammable Implantable intrathecal infusion pump, nonprogrammable Implantable intrathecal infusion pump, nonprogrammable Implantable intrathecal infusion pump, nonprogrammable Implantable intrathecal infusion pump, nonprogrammable Implantable intrathecal infusion pump, nonprogrammable Implantable intrathecal infusion pump, nonprogrammable Implantable intrathecal infusion pump, nonprogrammable Implantable intrathecal infusion pump, nonprogrammable

• Primary Device ID: 10886704044093
• NIH Device Record Key: 55799a39-6771-4988-89b0-7b01764a562e
• Commercial Distribution Discontinuation: 2017-09-28
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: CODMAN
• Version Model Number: IP40812
• Catalog Number: IP40812
• Company DUNS: 607846297
• Company Name: Cerenovus, 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: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• 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
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10886704044093 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P800036

FDA Product Code

• LKK: PUMP, INFUSION, IMPLANTED, PROGRAMMABLE

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2023-09-15
• Device Publish Date: 2014-09-20

On-Brand Devices [CODMAN]

• 10886704072614: CODMAN Power Cord Hospital Grade
• 10886704044093: MODEL 400 REFILL TUBING SET
• 10886704043447: CODMAN PPG (HONEYWELL RM 300) 10 Pin Interface Cable
• 10886704039204: CODMAN SPETZLER Non Stick Mirror Finish Bayonet Bipolar Forceps 0.9mm Angle Down Tip 25cm
• 10886704039198: CODMAN SPETZLER Non Stick Mirror Finish Bayonet Bipolar Forceps 0.9mm Tip 25cm