| Primary Device ID | 30815112021260 |
| NIH Device Record Key | aa3f5d62-de36-488f-8eb7-2b39d74acab1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Protocol Accessory Cart |
| Version Model Number | 390305 |
| Catalog Number | 390305 |
| 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 | false |
| Lot Batch | true |
| Serial Number | true |
| 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 | 609-514-2200 |
| xx@xx.xx | |
| Phone | 609-514-2200 |
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| Phone | 609-514-2200 |
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| Phone | 609-514-2200 |
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| Phone | 609-514-2200 |
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| 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 | |
| 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 | 10815112021266 [Primary] |
| GS1 | 30815112021260 [Package] Contains: 10815112021266 Package: Box [1 Units] In Commercial Distribution |
| 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 | 2023-07-17 |
| Device Publish Date | 2023-07-07 |
| 30815112021390 - CardioGen-82 Infusion System Model 1700 | 2023-12-11 Infusion system for Rubidium-82 saline injection. |
| 30815112021352 - CardioGen Patient Administration Set | 2023-10-24 Patient Administration Set for use with CardioGen-82 Infusion System |
| 30815112021369 - Vented Cap for Waste Bottle | 2023-10-24 Vented Cap for Waste Bottle for use with CardioGen-82 Infusion System |
| 30815112021376 - Waste Bottle | 2023-10-24 Waste Bottle for use with CardioGen-82 Infusion System |
| 30815112021239 - Protocol Touch Colon Insufflator | 2023-09-08 Protocol Touch Colon Insufflator |
| 30815112021253 - DIN 477 High Pressure Hose for CO2 | 2023-09-08 DIN Connector |
| 30815112021291 - High Pressure Hose and Yoke | 2023-09-08 High Pressure Hose and Yoke |
| 10815112020016 - Fluid Administration Set | 2023-07-28 Large Bore Tubing Administration Set |