Finger pulse oximeter

GUDID 06944249300009

Shenzhen Kingyield Technology Co., Ltd.

Pulse oximeter, battery-powered

• Primary Device ID: 06944249300009
• NIH Device Record Key: 3d80a158-3d02-4b08-9e22-adaf49dcde2a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Finger pulse oximeter
• Version Model Number: JB7239
• Company DUNS: 545348500
• Company Name: Shenzhen Kingyield 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: true
• Serial Number: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	06944249300009 [Package]; Contains: 06944249301211; Package: [24 Units]; In Commercial Distribution
GS1	06944249301211 [Primary]

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: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-15

On-Brand Devices [Finger pulse oximeter]

• 06944249300023: JB7649
• 06944249300016: SKU#349771
• 06944249300009: JB7239
• 06944249302621: FSA7649CM
• 06944249302607: DRL7649