QVC

GUDID 50822383005350

Respiratory Pulse Oximeters Product Description Fingertip Pulse Oximeter 1/ea

Drive Devilbiss Healthcare

Pulse Co-oximeter Pulse Co-oximeter Pulse Co-oximeter Pulse Co-oximeter Pulse Co-oximeter Pulse Co-oximeter Pulse Co-oximeter Pulse Co-oximeter Pulse Co-oximeter Pulse Co-oximeter Pulse Co-oximeter Pulse Co-oximeter Pulse Co-oximeter Pulse Co-oximeter Pulse Co-oximeter Pulse Co-oximeter Pulse Co-oximeter Pulse Co-oximeter Pulse Co-oximeter Pulse Co-oximeter Pulse Co-oximeter Pulse Co-oximeter Pulse Co-oximeter Pulse Co-oximeter Pulse Co-oximeter Pulse Co-oximeter Pulse Co-oximeter Pulse Co-oximeter 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