ByFloProducts

GUDID 10628693098035

Non-contact Infrared Thermometer

Byflo Products Inc.

Infrared patient thermometer, skin

• Primary Device ID: 10628693098035
• NIH Device Record Key: b46b6136-d434-41f8-94ac-7997c1775831
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ByFloProducts
• Version Model Number: JXB-178
• Company DUNS: 208296406
• Company Name: Byflo Products Inc.
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00628693098038 [Primary]
GS1	10628693098035 [Package]; Contains: 00628693098038; Package: Box [50 Units]; In Commercial Distribution

FDA Product Code

• FLL: Thermometer, Electronic, Clinical

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: 2022-02-28
• Device Publish Date: 2022-02-18

On-Brand Devices [ByFloProducts]

• 00628693098014: Infrared Forehead Thermometer
• 10628693098035: Non-contact Infrared Thermometer
• 10628693098042: Pulse Oximeter