Elution Test Vial Shield

GUDID 30815112021383

Elution Test Vial Shield for use with CardioGen-82 Infusion System

BRACCO DIAGNOSTICS INC

Vial radiation shield
Primary Device ID30815112021383
NIH Device Record Key452574d8-7655-46d0-8e4e-b751499c581a
Commercial Distribution StatusIn Commercial Distribution
Brand NameElution Test Vial Shield
Version Model Number001550
Company DUNS849234661
Company NameBRACCO DIAGNOSTICS INC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Producttrue
Single Usefalse
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

Device Identifiers

Device Issuing AgencyDevice ID
GS130815112021383 [Primary]

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 Date2023-07-03
Device Publish Date2023-06-23

On-Brand Devices [Elution Test Vial Shield]

10815112020085Elution Test Vial Shield for use with CardioGen-82 Infusion System
30815112021383Elution Test Vial Shield for use with CardioGen-82 Infusion System

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