| Primary Device ID | 06920485305787 |
| NIH Device Record Key | ee883203-0dd6-4c0f-9a3a-c2af058012f7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BOTHEALTH |
| Version Model Number | BSX578 |
| Company DUNS | 551105453 |
| Company Name | Shenzhen BSX Technology Electronics Co., Ltd. |
| 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 | true |
| 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 |
|---|---|
| GS1 | 06920485305787 [Primary] |
| DXN | System, Measurement, Blood-Pressure, Non-Invasive |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-12-23 |
| Device Publish Date | 2019-12-14 |
| 06920485305831 | BSX583 |
| 06920485305251 | BSX525 |
| 06920485305169 | BSX516 |
| 06920485305954 | BSX595 |
| 06920485305930 | BSX593 |
| 06920485305237 | BSX523 |
| 06920485305879 | BSX587 |
| 06920485305794 | BSX579 |
| 06920485305787 | BSX578 |
| 06920485305725 | BSX572 |
| 06920485305688 | BSX568 |
| 06920485305633 | BSX563 |
| 06920485305619 | BSX561 |
| 06920485305589 | BSX558 |
| 06920485305565 | BSX556 |
| 06920485305534 | BSX553 |
| 06920485305381 | BSX538 |
| 06920485305268 | BSX526 |
| 06920485305190 | BSX519 |
| 06920485305152 | BSX515 |
| 06920485305138 | BSX513 |
| 06920485305084 | BSX508 |
| 06920485305053 | BSX505 |
| 06920485305015 | BSX501 |