JUMAX

GUDID 00860002217208

Upper Arm Electronic Blood Pressure Monitor

JUMAX HEALTHCARE LLC

Physiologic-monitoring defibrillation system

• Primary Device ID: 00860002217208
• NIH Device Record Key: 1961b280-a326-470e-93fe-e9bc2816ead5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: JUMAX
• Version Model Number: A27
• 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: 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: false

Customer Support Contacts

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860002217208 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K131558

FDA Product Code

• DXN: System, Measurement, Blood-Pressure, Non-Invasive

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: 2019-08-21
• Device Publish Date: 2019-08-13

On-Brand Devices [JUMAX]

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