Primary Device ID | 30815112020072 |
NIH Device Record Key | 6c058fac-2039-4f68-940d-72b8aef159e2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Elution Test Vial |
Version Model Number | 001530 |
Company DUNS | 849234661 |
Company Name | BRACCO DIAGNOSTICS INC |
Device Count | 25 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx | |
Phone | 800-447-6883 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00815112020071 [Unit of Use] |
GS1 | 30815112020072 [Primary] |
GS1 | 50815112020076 [Package] Package: [6 Units] In Commercial Distribution |
IWW | Shield, Vial |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-03-30 |
Device Publish Date | 2023-03-22 |
30815112020577 | Elution Test Vial for use with CardioGen-82 Infusion System |
30815112020072 | Elution Test Vial for use with CardioGen-82 Infusion System, Model 510 |