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 |