Primary Device ID | 06974239700007 |
NIH Device Record Key | 03711cd4-c5ac-4cb5-b3e9-aca05786c2fc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | daxin |
Version Model Number | EF-808NBS |
Company DUNS | 722481840 |
Company Name | Guangzhou Daxin health technology Co.,Ltd |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | MR Unsafe |
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 | 06974239700007 [Primary] |
GS1 | 16974239700004 [Package] Package: [1 Units] In Commercial Distribution |
GS1 | 26974239700001 [Package] Contains: 16974239700004 Package: [4 Units] In Commercial Distribution |
PUH | Analyzer, Body Composition, Exempt |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-07-02 |
Device Publish Date | 2021-06-24 |
16974239700677 - FOXXD | 2024-10-04 |
16974239700660 - Sealy | 2024-09-20 |
16974239700646 - FOXXD | 2024-08-09 |
16974239700653 - FOXXD | 2024-08-09 |
06974239702841 - innotech | 2024-04-05 |
16974239700639 - innotech | 2024-04-05 |
16974239700615 - Bytech | 2024-02-01 |
16974239700608 - Bytech | 2023-12-26 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
DAXIN 87057368 5590750 Live/Registered |
SHENZHEN ZHENGPINGOU COMMERCE AND TRADEC 2016-06-02 |
DAXIN 79048636 not registered Dead/Abandoned |
LOU DAXING 2007-12-27 |