Voss Coronary Bypass Vein Clamp

GUDID 00811304020089

Coronary Bypass Vein Clamp (non-sterile)

VM CARDIO VASCULAR, INC.

Vascular clamp, single-use

• Primary Device ID: 00811304020089
• NIH Device Record Key: e9e2888b-05e6-422a-b44d-a7d6d2b20caa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Voss Coronary Bypass Vein Clamp
• Version Model Number: 82931-NS
• Company DUNS: 799240457
• Company Name: VM CARDIO VASCULAR, 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: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00811304020089 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K885161

FDA Product Code

• DXC: Clamp, Vascular

Sterilization

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

[00811304020089]

Ethylene Oxide

[00811304020089]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-01-05

On-Brand Devices [Voss Coronary Bypass Vein Clamp]

• 00811304020089: Coronary Bypass Vein Clamp (non-sterile)
• 00811304020058: Coronary Bypass Vein Clamp