| Primary Device ID | B146ER9WCNC0 |
| NIH Device Record Key | f5e4b3dd-432d-4ab5-afd3-504c9a65703e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ER9W CDMA wEvent |
| Version Model Number | 900-0612-01 |
| Company DUNS | 049529118 |
| Company Name | BRAEMAR MANUFACTURING, 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 | false |
| 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 Issuing Agency | Device ID |
|---|---|
| HIBCC | B146ER9WCNC0 [Primary] |
| DRG | Transmitters And Receivers, Physiological Signal, Radiofrequency |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-07-23 |
| Device Publish Date | 2020-07-15 |
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