Vasoview Hemopro VH-3000

GUDID 00607567700345

Vasoview Hemopro

MAQUET CARDIOVASCULAR LLC

Flexible endoscopic scissors, reusable Flexible endoscopic scissors, reusable Flexible endoscopic scissors, reusable

• Primary Device ID: 00607567700345
• NIH Device Record Key: 4cbceb36-cc9d-4acb-a231-b1f7db1681d8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vasoview Hemopro
• Version Model Number: VH-3000
• Catalog Number: VH-3000
• 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	00607567700345 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K052274

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

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: 2018-07-06
• Device Publish Date: 2016-09-24

On-Brand Devices [Vasoview Hemopro]

• 00607567701250: Vasoview Hemopro
• 00607567700345: Vasoview Hemopro