| Primary Device ID | 36941512150942 |
| NIH Device Record Key | 3b3850c5-e843-493f-ab96-122f9a776895 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Disposable IV Catheter |
| Version Model Number | IVC07-26 |
| Company DUNS | 421062164 |
| Company Name | Shinva Ande Healthcare Apparatus Co., Ltd |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 16941512150948 [Primary] |
| GS1 | 36941512150942 [Package] Contains: 16941512150948 Package: box [50 Units] In Commercial Distribution |
| GS1 | 56941512150946 [Package] Package: case [4 Units] In Commercial Distribution |
| FOZ | Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-05-16 |
| Device Publish Date | 2023-05-08 |
| 36941512151086 | IVC09-26 |
| 36941512151079 | IVC09-24 |
| 36941512151062 | IVC09-22 |
| 36941512151055 | IVC09-20 |
| 36941512151048 | IVC09-18 |
| 36941512151031 | IVC09-16 |
| 36941512151024 | IVC09-14 |
| 36941512150942 | IVC07-26 |
| 36941512150935 | IVC07-24 |
| 36941512150928 | IVC07-22 |
| 36941512150911 | IVC07-20 |
| 36941512150904 | IVC07-18 |
| 36941512150898 | IVC07-16 |
| 36941512150881 | IVC07-14 |