VEINCAS

GUDID 06971141530227

Shenzhen Vivolight Medical Device & Technology Co., Ltd.

Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator

• Primary Device ID: 06971141530227
• NIH Device Record Key: e9ed55eb-9e39-442c-8aa5-08270bc8ba26
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VEINCAS
• Version Model Number: V800NV
• Company DUNS: 543028475
• Company Name: Shenzhen Vivolight Medical Device & Technology Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06971141530227 [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: 2023-04-28
• Device Publish Date: 2023-04-20