Feverscan Large

GUDID 00815236021008

Reusable Liquid Crystal Forehead Thermometer

LCR HALLCREST, LLC.

Liquid-crystal patient thermometer, reusable

• Primary Device ID: 00815236021008
• NIH Device Record Key: 03759d4e-24e3-4338-b216-88969ab5652a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Feverscan Large
• Version Model Number: 1002 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: true
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: 847-998-8580
• Email: orders@hallcrest.com
• Phone: 847-998-8580
• Email: orders@hallcrest.com
• Phone: 847-998-8580
• Email: orders@hallcrest.com

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Optimal Storage and Handling Conditions: 60 to 80°F and 40 to 60% relative humidity
• Special Storage Condition, Specify: Between 0 and 0 *Optimal Storage and Handling Conditions: 60 to 80°F and 40 to 60% relative humidity
• Special Storage Condition, Specify: Between 0 and 0 *Optimal Storage and Handling Conditions: 60 to 80°F and 40 to 60% relative humidity

Device Identifiers

Device Issuing Agency	Device ID
GS1	00815236021008 [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: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-02-24
• Device Publish Date: 2019-01-15

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