Primary Device ID | 03610230007099 |
NIH Device Record Key | ff0560f3-e746-453b-9e38-b05314b30340 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Yumizen C1200 LDL Direct |
Version Model Number | 1300023857 |
Company DUNS | 273647420 |
Company Name | HORIBA ABX SAS |
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 | false |
Expiration Date | true |
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 | 03610230007099 [Primary] |
LBR | Ldl & Vldl Precipitation, Hdl |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-09-07 |
Device Publish Date | 2020-08-28 |
03610230004890 - ABX PENTRA ALP CP | 2023-07-06 |
03610230004913 - ABX PENTRA AMYLASE CP | 2023-07-06 |
03610230004920 - ABX PENTRA AST CP | 2023-07-06 |
03610230004937 - ABX PENTRA GGT CP | 2023-07-06 |
03610230004944 - ABX PENTRA LIPASE CP | 2023-07-06 |
03610230004975 - ABX PENTRA CHOLESTEROL CP | 2023-07-06 |
03610230004982 - ABX PENTRA BILIRUBIN, DIRECT CP | 2023-07-06 |
03610230004999 - ABX PENTRA HDL DIRECT CP | 2023-07-06 |