ALB AB362

GUDID 05055273200041

An Albumin test system is a device intended for the quantitative in vitro determination of Albumin concentration in serum and plasma.

RANDOX LABORATORIES LIMITED

Albumin IVD, reagent
Primary Device ID05055273200041
NIH Device Record Key6064fc3c-df5e-4b2b-8a55-5077bc3d506c
Commercial Distribution StatusIn Commercial Distribution
Brand NameALB
Version Model NumberAB362
Catalog NumberAB362
Company DUNS227530649
Company NameRANDOX LABORATORIES LIMITED
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+442894451070
Emailtechnical.services@randox.com

Operating and Storage Conditions

Storage Environment TemperatureBetween 15 Degrees Celsius and 25 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS105055273200041 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

CIXBromcresol Green Dye-Binding, Albumin

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-16

On-Brand Devices [ALB]

05055273208115An Albumin test system is a device intended for the quantitative in vitro determination of Album
05055273200058An Albumin test system is a device intended for the quantitative in vitro determination of Album
05055273200041An Albumin test system is a device intended for the quantitative in vitro determination of Album
05055273200034An Albumin test system is a device intended for the quantitative in vitro determination of Album

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