Vasoshield VH-5001

GUDID 00607567700462

Vasoshield Pressure Controlling Syringe

MAQUET CARDIOVASCULAR LLC

Vascular irrigation cannula, cardiac vessel graft

• Primary Device ID: 00607567700462
• NIH Device Record Key: d3327ffb-963a-45a3-b776-7a243224e697
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vasoshield
• Version Model Number: VH-5001
• Catalog Number: VH-5001
• Company DUNS: 022348156
• Company Name: MAQUET CARDIOVASCULAR LLC
• 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: 888-880-2874
• Email: cssurgery@maquet.com
• Phone: 888-880-2874
• Email: cssurgery@maquet.com
• Phone: 888-880-2874
• Email: cssurgery@maquet.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00607567700462 [Package]; Contains: 00607567700468; Package: 5 pack box [5 Units]; Discontinued: 2018-05-29; Not in Commercial Distribution
GS1	00607567700468 [Primary]
GS1	20607567700462 [Package]; Contains: 00607567700468; Package: 5 pack box [5 Units]; In Commercial Distribution

FDA Product Code

• GBX: Catheter, Irrigation

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-02-21
• Device Publish Date: 2016-09-24

On-Brand Devices [Vasoshield ]

• 00607567700462: Vasoshield Pressure Controlling Syringe
• 00607567700468: Vasoshield Pressure Controlling Syringe