Curlin IV Pump System

GUDID 18148440000361

ZEVEX INTERNATIONAL, INC.

Patient-controlled analgesia infusion pump

• Primary Device ID: 18148440000361
• NIH Device Record Key: d8e11a8e-c368-4e85-b2aa-0f83d0a7c26a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Curlin IV Pump System
• Version Model Number: Curlin Pump
• Company DUNS: 612746933
• Company Name: ZEVEX INTERNATIONAL, 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: false
• Lot Batch: false
• Serial Number: true
• 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: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	18148440000361 [Primary]

FDA Product Code

• FRN: Pump, Infusion

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-10-21

On-Brand Devices [Curlin IV Pump System]

• 18148440000361: Curlin Pump
• 30814844000376: Curlin IV Pump System