AccuVein

GUDID 00850019808018

Infrared Vein Visualization Device

Accuvein Inc.

Infrared-light vein locator

• Primary Device ID: 00850019808018
• NIH Device Record Key: b593d6ab-968c-4626-b218-d8f2e857fd19
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AccuVein
• Version Model Number: AV500
• Company DUNS: 807920546
• Company Name: Accuvein Inc.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: true
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• 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	00850019808018 [Primary]

FDA Product Code

• KZA: Device, Vein Location, Liquid Crystal

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-03-22
• Device Publish Date: 2021-03-12

On-Brand Devices [AccuVein]

• 00850019808032: Hands-Free Wheeled Stand
• 00850019808025: Powered Hands-Free Wheeled Stand
• 00850019808018: Infrared Vein Visualization Device
• 00850019808049: Hands-Free Arm with clamp
• 00850019808070: Powered, Goose Neck Hands-Free Wheeled Stand