Therasound EVO - 220V

GUDID 00092237901229

Therasound EVO Device Only (220V)

Compass Richmar, LLC

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• Primary Device ID: 00092237901229
• NIH Device Record Key: 35acdcff-99b5-481b-b069-537e1b86717c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Therasound EVO - 220V
• Version Model Number: 410-028
• Company DUNS: 080930531
• Company Name: Compass Richmar, 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: false
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 1-888-549-4945
• Email: customerservice@richmarweb.com
• Phone: 1-888-549-4945
• Email: customerservice@richmarweb.com
• Phone: 1-888-549-4945
• Email: customerservice@richmarweb.com
• Phone: 1-888-549-4945
• Email: customerservice@richmarweb.com
• Phone: 1-888-549-4945
• Email: customerservice@richmarweb.com
• Phone: 1-888-549-4945
• Email: customerservice@richmarweb.com
• Phone: 1-888-549-4945
• Email: customerservice@richmarweb.com
• Phone: 1-888-549-4945
• Email: customerservice@richmarweb.com
• Phone: 1-888-549-4945
• Email: customerservice@richmarweb.com
• Phone: 1-888-549-4945
• Email: customerservice@richmarweb.com
• Phone: 1-888-549-4945
• Email: customerservice@richmarweb.com
• Phone: 1-888-549-4945
• Email: customerservice@richmarweb.com
• Phone: 1-888-549-4945
• Email: customerservice@richmarweb.com
• Phone: 1-888-549-4945
• Email: customerservice@richmarweb.com
• Phone: 1-888-549-4945
• Email: customerservice@richmarweb.com
• Phone: 1-888-549-4945
• Email: customerservice@richmarweb.com
• Phone: 1-888-549-4945
• Email: customerservice@richmarweb.com
• Phone: 1-888-549-4945
• Email: customerservice@richmarweb.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00092237901229 [Primary]

FDA Product Code

• IMI: Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat

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: 2018-10-29
• Device Publish Date: 2018-09-27

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