| Primary Device ID | 14582231462893 |
| NIH Device Record Key | 914021e3-1ffb-4e5d-a772-443d4277e4d2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Cryotop US(G) |
| Version Model Number | Cryotop US(G) |
| Catalog Number | 81171 |
| 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 | 04582231462896 [Primary] |
| GS1 | 14582231462893 [Package] Contains: 04582231462896 Package: [10 Units] In Commercial Distribution |
| MQK | LABWARE, ASSISTED REPRODUCTION |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2020-01-08 |
| Device Publish Date | 2018-07-30 |
| 14580745043782 - ET CATHETER RYDEN | 2025-09-25 |
| 14580745043904 - ET CATHETER RYDEN | 2025-09-25 |
| 14580745044239 - ET CATHETER RYDEN | 2025-09-25 |
| 14580745044246 - ET CATHETER RYDEN | 2025-09-25 |
| 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 |