Blue Jay

GUDID 06942820461668

Fingertip Pulse Oximeter

Beijing Choice Electronic Technology Co., Ltd.

Pulse oximeter, battery-powered

• Primary Device ID: 06942820461668
• NIH Device Record Key: ee723224-487c-47cb-8c3e-4d419ae4b03a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Blue Jay
• Version Model Number: BJ240120
• Company DUNS: 526882823
• Company Name: Beijing Choice Electronic Technology Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	06942820461668 [Primary]

FDA Product Code

• OCH: Oximeter, Infrared, Sporting, Aviation

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-11-17

On-Brand Devices [Blue Jay]

• 00846841060755: Fully Automatic Digital Wrist Blood Pressure Monitor
• 06942820461675: Fingertip Pulse Oximeter
• 06942820461668: Fingertip Pulse Oximeter
• 06942820461422: Fingertip Pulse Oximeter
• 06942820461415: Fingertip Pulse Oximeter
• 06942820462016: BLUE JAY Arm Blood Pressure Monitor BJ120108