Alinity 09P5202

GUDID 00380740179359

Alinity c Benzodiazepines Semiquant Calibrator Kit

ABBOTT LABORATORIES

Multiple drugs of abuse IVD, calibrator Multiple drugs of abuse IVD, calibrator Multiple drugs of abuse IVD, calibrator
Primary Device ID00380740179359
NIH Device Record Key7df11fe0-fbff-4fd8-9700-8c391d644a25
Commercial Distribution StatusIn Commercial Distribution
Brand NameAlinity
Version Model Number09P5202
Catalog Number09P5202
Company DUNS079226220
Company NameABBOTT LABORATORIES
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usefalse
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+1(877)422-2688
Emailxx@xx.xx
Phone+1(877)422-2688
Emailxx@xx.xx
Phone+1(877)422-2688
Emailxx@xx.xx

Operating and Storage Conditions

Storage Environment TemperatureBetween 2 Degrees Celsius and 8 Degrees Celsius
Handling Environment TemperatureBetween 0 and 30 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 8 Degrees Celsius
Handling Environment TemperatureBetween 0 and 30 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 8 Degrees Celsius
Handling Environment TemperatureBetween 0 and 30 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS100380740179359 [Primary]
GS100380740179359 [Primary]
GS100380740179359 [Primary]

FDA Product Code

DKBCalibrators, drug mixture
DKBCalibrators, drug mixture
DKBCalibrators, drug mixture

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-05-19
Device Publish Date2020-05-11

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