Virtuox

GUDID 00817698020018

VPOD Ultra, wrist pulse oximeter

HEALTHCARE LOGISTICS SYSTEMS LLC

Pulse oximeter, battery-powered Pulse oximeter, battery-powered Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter

• Primary Device ID: 00817698020018
• NIH Device Record Key: 4197e0cf-2067-43a1-bb32-c86c002cea1c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Virtuox
• Version Model Number: 1000
• Company DUNS: 079452927
• Company Name: HEALTHCARE LOGISTICS SYSTEMS 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: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• 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

Customer Support Contacts

• Phone: 877-337-7111
• Email: sales@virtuox.net
• Phone: 877-337-7111
• Email: sales@virtuox.net
• Phone: 877-337-7111
• Email: sales@virtuox.net
• Phone: 877-337-7111
• Email: sales@virtuox.net
• Phone: 877-337-7111
• Email: sales@virtuox.net
• Phone: 877-337-7111
• Email: sales@virtuox.net
• Phone: 877-337-7111
• Email: sales@virtuox.net
• Phone: 877-337-7111
• Email: sales@virtuox.net
• Phone: 877-337-7111
• Email: sales@virtuox.net
• Phone: 877-337-7111
• Email: sales@virtuox.net
• Phone: 877-337-7111
• Email: sales@virtuox.net
• Phone: 877-337-7111
• Email: sales@virtuox.net
• Phone: 877-337-7111
• Email: sales@virtuox.net
• Phone: 877-337-7111
• Email: sales@virtuox.net
• Phone: 877-337-7111
• Email: sales@virtuox.net
• Phone: 877-337-7111
• Email: sales@virtuox.net
• Phone: 877-337-7111
• Email: sales@virtuox.net

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817698020018 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K090671

FDA Product Code

• DQA: Oximeter

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-12-07

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