JUMAX

GUDID 00860002217222

Infrared Ear/Forehead Thermometer

JUMAX HEALTHCARE LLC

Infrared patient thermometer, ear/skin

• Primary Device ID: 00860002217222
• NIH Device Record Key: 033bd828-e123-4e22-aa39-99f76184d284
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: JUMAX
• Version Model Number: AT11
• Company DUNS: 117115861
• Company Name: JUMAX HEALTHCARE LLC
• 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

Customer Support Contacts

• Phone: 9166217548
• Email: antoine.ju@jumaxhc.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860002217222 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K182597

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: 2019-12-05
• Device Publish Date: 2019-11-27

On-Brand Devices [JUMAX]

• 00860002217222: Infrared Ear/Forehead Thermometer
• 00860002217208: Upper Arm Electronic Blood Pressure Monitor