FeverScan Ultra

GUDID 00815236021022

Reusable Liquid Crystal Forehead Thermometer - 12 Event, Dual Scale, with Blank Tabs

LCR HALLCREST, LLC.

Liquid-crystal patient thermometer, reusable

• Primary Device ID: 00815236021022
• NIH Device Record Key: 6c50a0d8-3e63-4d46-b3be-3c03150685d8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FeverScan Ultra
• Version Model Number: 1026 NDP
• Company DUNS: 059247507
• Company Name: LCR HALLCREST, LLC.
• 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: 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: 847-998-8580
• Email: orders@hallcrest.com

Operating and Storage Conditions

• Storage Environment Temperature: Between 60 Degrees Fahrenheit and 104 Degrees Fahrenheit

Device Identifiers

Device Issuing Agency	Device ID
GS1	00815236021022 [Primary]

FDA Product Code

• KPD: Strip, Temperature, Forehead, Liquid Crystal

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: 2020-04-21
• Device Publish Date: 2020-04-13

On-Brand Devices [FeverScan Ultra]

• 00815236020919: Reusable Forehead Thermometer
• 00815236020391: FeverScan Ultra Reusable Forehead Thermometer
• 00815236021039: Reusable Liquid Crystal Forehead Thermometer - 12 Event, Celsius only with Blank Tabs
• 00815236021022: Reusable Liquid Crystal Forehead Thermometer - 12 Event, Dual Scale, with Blank Tabs