Primary Device ID | 05055273200041 |
NIH Device Record Key | 6064fc3c-df5e-4b2b-8a55-5077bc3d506c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ALB |
Version Model Number | AB362 |
Catalog Number | AB362 |
Company DUNS | 227530649 |
Company Name | RANDOX LABORATORIES LIMITED |
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 | true |
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 | true |
OTC Over-The-Counter | false |
Phone | +442894451070 |
technical.services@randox.com |
Storage Environment Temperature | Between 15 Degrees Celsius and 25 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05055273200041 [Primary] |
CIX | Bromcresol Green Dye-Binding, Albumin |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-16 |
05055273208115 | An Albumin test system is a device intended for the quantitative in vitro determination of Album |
05055273200058 | An Albumin test system is a device intended for the quantitative in vitro determination of Album |
05055273200041 | An Albumin test system is a device intended for the quantitative in vitro determination of Album |
05055273200034 | An Albumin test system is a device intended for the quantitative in vitro determination of Album |