ProHT

GUDID 00001245890032

Inland Products, Inc.

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• Primary Device ID: 00001245890032
• NIH Device Record Key: 635e454f-4275-4e1f-94d9-f9e39bfce019
• Commercial Distribution Discontinuation: 2019-12-31
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: ProHT
• Version Model Number: JPD-FR200
• Company DUNS: 151304636
• Company Name: Inland Products, Inc.
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00001245890032 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K131243

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: 4
• Public Version Date: 2021-08-25
• Device Publish Date: 2016-08-17