VIRTUOX

GUDID 06942820462108

VIRTUOX Pulse Oximeter VPOD H PRO

Beijing Choice Electronic Technology Co., Ltd.

Pulse oximeter, line-powered

• Primary Device ID: 06942820462108
• NIH Device Record Key: ad4e0908-bf64-4ea4-b0b5-8bf4533383f7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VIRTUOX
• Version Model Number: VPOD H PRO
• Company DUNS: 526882823
• Company Name: Beijing Choice Electronic Technology Co., Ltd.
• 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: 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	06942820462108 [Primary]

FDA Product Code

• DQA: Oximeter

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: 2020-10-28
• Device Publish Date: 2020-10-20

On-Brand Devices [VIRTUOX]

• 06942820461767: Wrist Pulse Oximeter
• 06942820462115: VIRTUOX Vital Sign Monitor VPOD VITAL PRO
• 06942820462108: VIRTUOX Pulse Oximeter VPOD H PRO