Primary Device ID | 10815112020153 |
NIH Device Record Key | 52bc450b-b3c7-43ac-8176-1ab8fecc1110 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Protocol Touch Administration Set with Small Catheter and Retention Cuff |
Version Model Number | 390309 |
Catalog Number | 390309 |
Company DUNS | 849234661 |
Company Name | BRACCO DIAGNOSTICS INC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 609-514-2200 |
xx@xx.xx | |
Phone | 609-514-2200 |
xx@xx.xx | |
Phone | 609-514-2200 |
xx@xx.xx | |
Phone | 609-514-2200 |
xx@xx.xx | |
Phone | 609-514-2200 |
xx@xx.xx | |
Phone | 609-514-2200 |
xx@xx.xx | |
Phone | 609-514-2200 |
xx@xx.xx | |
Phone | 609-514-2200 |
xx@xx.xx | |
Phone | 609-514-2200 |
xx@xx.xx | |
Phone | 609-514-2200 |
xx@xx.xx | |
Phone | 609-514-2200 |
xx@xx.xx | |
Phone | 609-514-2200 |
xx@xx.xx | |
Phone | 609-514-2200 |
xx@xx.xx | |
Phone | 609-514-2200 |
xx@xx.xx | |
Phone | 609-514-2200 |
xx@xx.xx | |
Phone | 609-514-2200 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10815112020153 [Primary] |
GS1 | 30815112020157 [Package] Package: Box [24 Units] In Commercial Distribution |
FCX | Insufflator, Automatic Carbon-Dioxide For Endoscope |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-06-30 |
Device Publish Date | 2016-09-19 |
10815112020153 | Protocol Touch Administration Set we/20fr. Tip |
30815112021246 | Protocol Touch Administration Set w/20 Fr. Tip |