QVC

GUDID 50822383005350

Respiratory Pulse Oximeters Product Description Fingertip Pulse Oximeter 1/ea

Drive Devilbiss Healthcare

Pulse Co-oximeter

• Primary Device ID: 50822383005350
• NIH Device Record Key: 3be79dbb-ba74-4fb5-920c-09f8011fe826
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: QVC
• Version Model Number: Q-MQ3000
• Company DUNS: 867673159
• Company Name: Drive Devilbiss Healthcare
• Device Count: 2
• DM Exempt: true
• 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: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00822383005331 [Primary]
GS1	50822383005350 [Unit of Use]

FDA Product Code

• OCH: oximeter, infrared, sporting, aviation

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: 2021-03-05
• Device Publish Date: 2021-02-25

On-Brand Devices [QVC]

• 50822383005350: Respiratory Pulse Oximeters Product Description Fingertip Pulse Oximeter 1/ea
• 00822383005355: Personal Care BP Monitor Product Description BPMonitor,Wrist,Auto,1EA,QVCBrnBx NoRetl