Elution Test Vial

GUDID 30815112020072

Elution Test Vial for use with CardioGen-82 Infusion System, Model 510

BRACCO DIAGNOSTICS INC

General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use General laboratory container, single-use
Primary Device ID30815112020072
NIH Device Record Key6c058fac-2039-4f68-940d-72b8aef159e2
Commercial Distribution StatusIn Commercial Distribution
Brand NameElution Test Vial
Version Model Number001530
Company DUNS849234661
Company NameBRACCO DIAGNOSTICS INC
Device Count25
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx
Phone800-447-6883
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS100815112020071 [Unit of Use]
GS130815112020072 [Primary]
GS150815112020076 [Package]
Package: [6 Units]
In Commercial Distribution

FDA Product Code

IWWShield, Vial

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-03-30
Device Publish Date2023-03-22

On-Brand Devices [Elution Test Vial ]

30815112020577Elution Test Vial for use with CardioGen-82 Infusion System
30815112020072Elution Test Vial for use with CardioGen-82 Infusion System, Model 510

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