Primary Device ID | 03610230006948 |
NIH Device Record Key | f3f76951-8cb9-4f2c-b5ab-347c4d42c3f1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Yumizen C1200 CK-NAC |
Version Model Number | 1300023841 |
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 | 03610230006948 [Primary] |
CGS | Nad Reduction/Nadh Oxidation, Cpk Or Isoenzymes |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-09-08 |
Device Publish Date | 2020-08-31 |
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