Thermotex

GUDID 00183470000302

Thermotex Therapy Systems Ltd.

Musculoskeletal infrared phototherapy unit, non-wearable

• Primary Device ID: 00183470000302
• NIH Device Record Key: 546e0087-ff34-46d7-b426-afea9b657bf1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Thermotex
• Version Model Number: Professional
• Company DUNS: 203727354
• Company Name: Thermotex Therapy Systems Ltd.
• 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	00183470000302 [Primary]

FDA Product Code

• IRT: Pad, Heating, Powered

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: 2023-10-02
• Device Publish Date: 2023-09-24

On-Brand Devices [Thermotex]

• 00183470000951: Foot
• 00183470000722: Neck
• 00183470000630: Wrist Left
• 00183470000616: Wrist Right
• 00183470000302: Professional
• 00183470000258: Platinum
• 00183470000203: Gold
• 00183470000104: Elbow
• 00183470000050: Knee