Primary Device ID | 03610230005583 |
NIH Device Record Key | 43b6a1c1-7e4c-4d18-aa03-1f4d8e1eabd2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CUVETTE SEGMENTS RACK |
Version Model Number | 1220001891 |
Company DUNS | 273647420 |
Company Name | HORIBA ABX SAS |
Device Count | 450 |
DM Exempt | false |
Pre-market Exempt | true |
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 | 03610230005583 [Primary] |
GS1 | 03610230008140 [Unit of Use] |
JJE | Analyzer, Chemistry (Photometric, Discrete), For Clinical Use |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2021-01-22 |
Device Publish Date | 2016-09-21 |
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