FREDS 76-352

GUDID 00084579114696

60 SECOND DIGITAL THERMOMETER

VERIDIAN HEALTHCARE LLC

Intermittent electronic patient thermometer

• Primary Device ID: 00084579114696
• NIH Device Record Key: 2a759fc1-2df4-493f-ae4f-9ae7fb6c4492
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FREDS
• Version Model Number: 76-352
• Catalog Number: 76-352
• Company DUNS: 830437997
• Company Name: VERIDIAN 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00084579114696 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K041516

FDA Product Code

• FLL: Thermometer, Electronic, Clinical

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2018-01-18

On-Brand Devices [FREDS]

• 00084579114696: 60 SECOND DIGITAL THERMOMETER
• 00084579114665: Automatic Digital Blood Pressure Monitor
• 00084579114658: AUTOMATIC WRIST BLOOD PRESSURE MONITOR