Thermophore Plus

GUDID 00040337012567

Medium Thermophore Plus

Battle Creek Equipment Co.

Electric pad localized-body heating system

• Primary Device ID: 00040337012567
• NIH Device Record Key: 5e2aa90b-4e75-4a45-acde-120df5483859
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Thermophore Plus
• Version Model Number: F00256
• Company DUNS: 001957422
• Company Name: Battle Creek Equipment Co.
• 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: true
• 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	00040337002568 [Primary]
GS1	00040337012567 [Package]; Contains: 00040337002568; Package: Case Pack [12 Units]; In Commercial Distribution

FDA Product Code

• IRT: Pad, Heating, Powered

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: 2020-07-07
• Device Publish Date: 2017-01-04

On-Brand Devices [Thermophore Plus]

• 00040337002773: Petite Thermophore Plus
• 00040337012567: Medium Thermophore Plus
• 00040337012550: Standard Thermophore Plus