Primary Device ID | 30815112021291 |
NIH Device Record Key | ee4b6ec0-f1c4-4899-b60e-939018eb61a1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | High Pressure Hose and Yoke |
Version Model Number | 710603 |
Catalog Number | 710603 |
Company DUNS | 849234661 |
Company Name | BRACCO DIAGNOSTICS INC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 30815112021291 [Primary] |
FCX | Insufflator, Automatic Carbon-Dioxide For Endoscope |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-09-08 |
Device Publish Date | 2023-08-31 |
30815112020799 | High Pressure Hose and Yoke |
30815112021291 | High Pressure Hose and Yoke |