Primary Device ID | 16953825907157 |
NIH Device Record Key | bee4d1de-8690-4567-91b7-9f1e7920a001 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BeBrig MED + |
Version Model Number | U82RH |
Catalog Number | Yes |
Company DUNS | 421294358 |
Company Name | Shenzhen Urion Technology 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 | false |
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 | 06953825907150 [Primary] |
GS1 | 16953825907157 [Package] Contains: 06953825907150 Package: Carton [20 Units] In Commercial Distribution |
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 | 2023-06-22 |
Device Publish Date | 2023-06-14 |
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16953825908833 - N/A | 2024-10-31 |
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16953825908802 - urion | 2024-10-22 |