| Primary Device ID | 14580745042211 |
| NIH Device Record Key | 7973a045-7f66-4b2a-9f45-0514f8c3f2a8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Kitazato ET Catheter |
| Version Model Number | 233335 |
| Catalog Number | 233335 |
| Company DUNS | 711091157 |
| Company Name | KITAZATO CORPORATION |
| 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 | true |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |