MC3 Crescent Jugular Dual Lumen Catheter 70130

GUDID 10854916006819

Dual Lumen ECMO Cannula

MICHIGAN CRITICAL CARE CONSULTANTS, INC.

Mobile extracorporeal gas exchange system catheter kit

• Primary Device ID: 10854916006819
• NIH Device Record Key: 7b9faa56-8cfd-4253-8113-ebcadd6b8888
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MC3 Crescent Jugular Dual Lumen Catheter
• Version Model Number: 70130
• Catalog Number: 70130
• Company DUNS: 806687406
• Company Name: MICHIGAN CRITICAL CARE CONSULTANTS, 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

Device Dimensions

• Catheter Gauge: 30 French

Device Identifiers

Device Issuing Agency	Device ID
GS1	10854916006819 [Previous]
GS1	10854916006949 [Primary]

FDA Product Code

• PZS: Dual Lumen Ecmo Cannula

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-10-21
• Device Publish Date: 2018-07-30

On-Brand Devices [MC3 Crescent Jugular Dual Lumen Catheter]

• 10854916006826: Dual Lumen ECMO Cannula
• 10854916006819: Dual Lumen ECMO Cannula
• 10854916006802: Dual Lumen ECMO Cannula
• 10854916006796: Dual Lumen ECMO Cannula
• 10854916006789: Dual Lumen ECMO Cannula