CODMAN ACCU-FLO HOLTER NS0326

GUDID 10886704045113

CODMAN ACCU-FLO Dotted Ventricular Catheter 15cm HOLTER SALMON-RICKHAM Reservoir Packaged with Stainless Steel Base for 6mm Burr Hole Includes: Stylet and Information Manual

CODMAN & SHURTLEFF, INC.

Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir

• Primary Device ID: 10886704045113
• NIH Device Record Key: 199d813f-5bb8-4491-841d-fc897aeec5a6
• Commercial Distribution Discontinuation: 2022-09-01
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CODMAN ACCU-FLO HOLTER
• Version Model Number: NS0326
• Catalog Number: NS0326
• 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	10886704045113 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K102961

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: 2022-01-26
• Device Publish Date: 2015-09-20

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