VAMP PLUS VP2

GUDID 07460691944831

BLOOD MANAGEMENT SYSTEM

Edwards Lifesciences LLC

Arterial blood sampling kit

• Primary Device ID: 07460691944831
• NIH Device Record Key: 9a3acf8a-8054-4c18-ac31-921f10c15473
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VAMP PLUS
• Version Model Number: VP2
• Catalog Number: VP2
• Company DUNS: 134139174
• Company Name: Edwards Lifesciences 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: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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: +1(800)822-9637
• Email: tech_support@edwards.com

Device Dimensions

• Length: 60 Inch

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *STORE IN A COOL, DRY PLACE.

Device Identifiers

Device Issuing Agency	Device ID
GS1	07460691944831 [Primary]
GS1	57460691944836 [Package]; Package: Shipper [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K181684

FDA Product Code

• KRA: Catheter, continuous flush

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: 2018-11-28
• Device Publish Date: 2016-09-03

On-Brand Devices [VAMP PLUS]

• 07460691958616: BLOOD MANAGEMENT SYSTEM
• 07460691955578: VAMP PLUS KIT - STERILE
• 07460691944831: BLOOD MANAGEMENT SYSTEM
• 07460691944824: BLOOD MANAGEMENT SYSTEM.