| Primary Device ID | D79261453 |
| NIH Device Record Key | a86bb01f-e4ff-4031-8ef5-5ae31ba66551 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Myotronics 6145 Duotrodes |
| Version Model Number | 6145 |
| Company DUNS | 053824652 |
| Company Name | MYOTRONICS NOROMED, 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Phone | 2062434214 |
| info@myotronics.com | |
| Phone | 2062434214 |
| info@myotronics.com | |
| Phone | 2062434214 |
| info@myotronics.com | |
| Phone | 2062434214 |
| info@myotronics.com | |
| Phone | 2062434214 |
| info@myotronics.com | |
| Phone | 2062434214 |
| info@myotronics.com | |
| Phone | 2062434214 |
| info@myotronics.com | |
| Phone | 2062434214 |
| info@myotronics.com | |
| Phone | 2062434214 |
| info@myotronics.com | |
| Phone | 2062434214 |
| info@myotronics.com | |
| Phone | 2062434214 |
| info@myotronics.com | |
| Phone | 2062434214 |
| info@myotronics.com | |
| Phone | 2062434214 |
| info@myotronics.com | |
| Phone | 2062434214 |
| info@myotronics.com | |
| Phone | 2062434214 |
| info@myotronics.com | |
| Phone | 2062434214 |
| info@myotronics.com | |
| Phone | 2062434214 |
| info@myotronics.com | |
| Phone | 2062434214 |
| info@myotronics.com |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | D79261451 [Primary] |
| HIBCC | D79261452 [Package] Contains: D79261451 Package: Box [15 Units] In Commercial Distribution |
| HIBCC | D79261453 [Package] Contains: D79261451 Package: Case [150 Units] In Commercial Distribution |
| IKN | Electromyograph, Diagnostic |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-19 |
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