Vasoview 7 XB, OUS VH-3200-W

GUDID 00607567700437

Vasoview 7 XB, OUS

MAQUET CARDIOVASCULAR LLC

Flexible endoscopic scissors, reusable

• Primary Device ID: 00607567700437
• NIH Device Record Key: f87fc982-3de6-4510-89f6-4a0650b9041b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vasoview 7 XB, OUS
• Version Model Number: VH-3200-W
• Catalog Number: VH-3200-W
• 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	00607567700437 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K041981

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

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