| Primary Device ID | 10815112020672 |
| NIH Device Record Key | 3c79edfd-6c16-496b-925e-f675699862d2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Protocol Touch Colon Insufflator |
| Version Model Number | 390308 |
| Catalog Number | 390308 |
| 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 | false |
| 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 |
| 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 | 10815112020672 [Primary] |
| GS1 | 30815112020676 [Package] 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 | 2021-09-21 |
| Device Publish Date | 2021-09-13 |
| 10815112020672 | Protocol Touch Insufflator |
| 30815112021239 | Protocol Touch Colon Insufflator |