ProAlert 570 ProAlert 570

GUDID 00860002736006

JERON ELECTRONIC SYSTEMS, INC.

Nurse call system

• Primary Device ID: 00860002736006
• NIH Device Record Key: 2961393c-3c20-4071-8346-8dab21de3ece
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ProAlert 570
• Version Model Number: ProAlert 570
• Catalog Number: ProAlert 570
• Company DUNS: 047024617
• Company Name: JERON ELECTRONIC SYSTEMS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• 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	00860002736006 [Primary]

FDA Product Code

• ILQ: System, Communication, Powered

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: 2020-02-18
• Device Publish Date: 2020-02-10

On-Brand Devices [ProAlert 570]

• 08600027360068: ProAlert 570
• 00860002736006: ProAlert 570