Curlin IV Pump System

GUDID 30814844000376

Curlin IV Pump System

ZEVEX INTERNATIONAL, INC.

Patient-controlled analgesia infusion pump Patient-controlled analgesia infusion pump Patient-controlled analgesia infusion pump Patient-controlled analgesia infusion pump Patient-controlled analgesia infusion pump Patient-controlled analgesia infusion pump Patient-controlled analgesia infusion pump Patient-controlled analgesia infusion pump Patient-controlled analgesia infusion pump Patient-controlled analgesia infusion pump Patient-controlled analgesia infusion pump Patient-controlled analgesia infusion pump Patient-controlled analgesia infusion pump Patient-controlled analgesia infusion pump Patient-controlled analgesia infusion pump Patient-controlled analgesia infusion pump Patient-controlled analgesia infusion pump Patient-controlled analgesia infusion pump Patient-controlled analgesia infusion pump Patient-controlled analgesia infusion pump Patient-controlled analgesia infusion pump Patient-controlled analgesia infusion pump Patient-controlled analgesia infusion pump Patient-controlled analgesia infusion pump Patient-controlled analgesia infusion pump Patient-controlled analgesia infusion pump Patient-controlled analgesia infusion pump Patient-controlled analgesia infusion pump Patient-controlled analgesia infusion pump Patient-controlled analgesia infusion pump Patient-controlled analgesia infusion pump
Primary Device ID30814844000376
NIH Device Record Key2c9e097f-4b7c-4312-822c-e7f1e06a41a6
Commercial Distribution StatusIn Commercial Distribution
Brand NameCurlin IV Pump System
Version Model NumberCurlin Pump
Company DUNS612746933
Company NameZEVEX INTERNATIONAL, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone800-970-2337
Emailmedcustomerservice@moog.com
Phone800-970-2337
Emailmedcustomerservice@moog.com
Phone800-970-2337
Emailmedcustomerservice@moog.com
Phone800-970-2337
Emailmedcustomerservice@moog.com
Phone800-970-2337
Emailmedcustomerservice@moog.com
Phone800-970-2337
Emailmedcustomerservice@moog.com
Phone800-970-2337
Emailmedcustomerservice@moog.com
Phone800-970-2337
Emailmedcustomerservice@moog.com
Phone800-970-2337
Emailmedcustomerservice@moog.com
Phone800-970-2337
Emailmedcustomerservice@moog.com
Phone800-970-2337
Emailmedcustomerservice@moog.com
Phone800-970-2337
Emailmedcustomerservice@moog.com
Phone800-970-2337
Emailmedcustomerservice@moog.com
Phone800-970-2337
Emailmedcustomerservice@moog.com
Phone800-970-2337
Emailmedcustomerservice@moog.com
Phone800-970-2337
Emailmedcustomerservice@moog.com
Phone800-970-2337
Emailmedcustomerservice@moog.com
Phone800-970-2337
Emailmedcustomerservice@moog.com
Phone800-970-2337
Emailmedcustomerservice@moog.com
Phone800-970-2337
Emailmedcustomerservice@moog.com
Phone800-970-2337
Emailmedcustomerservice@moog.com
Phone800-970-2337
Emailmedcustomerservice@moog.com
Phone800-970-2337
Emailmedcustomerservice@moog.com
Phone800-970-2337
Emailmedcustomerservice@moog.com
Phone800-970-2337
Emailmedcustomerservice@moog.com
Phone800-970-2337
Emailmedcustomerservice@moog.com
Phone800-970-2337
Emailmedcustomerservice@moog.com
Phone800-970-2337
Emailmedcustomerservice@moog.com
Phone800-970-2337
Emailmedcustomerservice@moog.com
Phone800-970-2337
Emailmedcustomerservice@moog.com
Phone800-970-2337
Emailmedcustomerservice@moog.com

Device Identifiers

Device Issuing AgencyDevice ID
GS110814844000365 [Primary]
GS118148440000361 [Previous]
GS130814844000376 [Package]
Contains: 10814844000365
Package: [1 Units]
In Commercial Distribution

FDA Product Code

FRNPump, Infusion

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-05-07
Device Publish Date2021-04-29

On-Brand Devices [Curlin IV Pump System]

18148440000361Curlin Pump
30814844000376Curlin IV Pump System

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