| Primary Device ID | B146ERWCD040 |
| NIH Device Record Key | 40e14fa6-0cf8-4af4-b3d5-9e2af2af3d70 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ER9W Cardiolabs |
| Version Model Number | 900-0612-04 |
| 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 | B146ERWCD040 [Primary] |
| DRG | Transmitters And Receivers, Physiological Signal, Radiofrequency |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-11-08 |
| Device Publish Date | 2019-10-08 |
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