| Primary Device ID | 14580303269500 |
| NIH Device Record Key | 0b5d4c3c-032e-4336-b019-8c1625e5d608 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Kitazato ET Catheter Type1-v5 EC-PRO Normal |
| Version Model Number | 205018 Type1-v5 EC-PRO Normal |
| Catalog Number | 205018 |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04580303269503 [Primary] |
| GS1 | 14580303269500 [Package] Contains: 04580303269503 Package: [10 Units] In Commercial Distribution |
| MQF | CATHETER, ASSISTED REPRODUCTION |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-03-11 |
| Device Publish Date | 2019-02-07 |
| 14573316384773 - Ultra-Fast Warm | 2025-09-05 |
| 14573316385107 - Ultra-Fast Vitri | 2025-09-05 |
| 14573316385114 - Ultra-Fast Vitri | 2025-09-05 |
| 14573316385978 - Ultra-Fast Vitri | 2025-09-05 |
| 14573316385985 - Ultra-Fast Vitri | 2025-09-05 |
| 14573316386012 - Ultra-Fast Vitri | 2025-09-05 |
| 14573316386029 - Ultra-Fast Vitri | 2025-09-05 |
| 14573316386173 - ES(Equilibration Solution) Pack 4 vials | 2024-12-03 ES(Equilibration Solution) Pack 4x1.5ml vials |