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 |
Phone | 1-888-549-4945 |
customerservice@richmarweb.com | |
Phone | 1-888-549-4945 |
customerservice@richmarweb.com | |
Phone | 1-888-549-4945 |
customerservice@richmarweb.com | |
Phone | 1-888-549-4945 |
customerservice@richmarweb.com | |
Phone | 1-888-549-4945 |
customerservice@richmarweb.com | |
Phone | 1-888-549-4945 |
customerservice@richmarweb.com | |
Phone | 1-888-549-4945 |
customerservice@richmarweb.com | |
Phone | 1-888-549-4945 |
customerservice@richmarweb.com | |
Phone | 1-888-549-4945 |
customerservice@richmarweb.com | |
Phone | 1-888-549-4945 |
customerservice@richmarweb.com | |
Phone | 1-888-549-4945 |
customerservice@richmarweb.com | |
Phone | 1-888-549-4945 |
customerservice@richmarweb.com | |
Phone | 1-888-549-4945 |
customerservice@richmarweb.com | |
Phone | 1-888-549-4945 |
customerservice@richmarweb.com | |
Phone | 1-888-549-4945 |
customerservice@richmarweb.com | |
Phone | 1-888-549-4945 |
customerservice@richmarweb.com | |
Phone | 1-888-549-4945 |
customerservice@richmarweb.com | |
Phone | 1-888-549-4945 |
customerservice@richmarweb.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00092237901229 [Primary] |
IMI | Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat |
Steralize Prior To Use | false |
Device Is Sterile | false |
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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