Primary Device ID | 06971209160120 |
NIH Device Record Key | fd6fe976-4231-4b42-a046-5e1a3bdd4de2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Aleshon |
Version Model Number | B1682 |
Company DUNS | 418012517 |
Company Name | Shenzhen Yuezhongxing 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 | 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 |
---|---|
GS1 | 06971209160120 [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 | 2023-07-27 |
Device Publish Date | 2023-07-19 |
06971209160038 | W1681 |
06971209160021 | W202 |
06971209160014 | W203 |
06971209160069 | W1681BL |
06971209160052 | W202BL |
06971209160045 | W203BL |
06971209160076 | BM100-EN |
06971209160090 | MY126 |
06971209160083 | MY123 |
06971209160182 | 222BT |
06971209160175 | 222 |
06971209160168 | W1681BT |
06971209160151 | W1681R |
06971209160144 | 121 |
06971209160137 | B1683 |
06971209160120 | B1682 |
06971209160113 | B1681 |
06971209160106 | 111 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ALESHON 87881371 5621928 Live/Registered |
Shenzhen Yuezhongxing Technology Co., Ltd. 2018-04-17 |