| Primary Device ID | 06936841208098 |
| NIH Device Record Key | 6ec9d284-8c8f-4c79-b355-59d27bb76a21 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | IV cannula |
| Version Model Number | II-B-18G |
| Catalog Number | 175005 |
| Company DUNS | 418642903 |
| Company Name | Tianck Medical Co., Ltd. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06936841208098 [Primary] |
| GS1 | 16936841208095 [Package] Package: middle package [125 Units] In Commercial Distribution |
| GS1 | 26936841208092 [Package] Contains: 16936841208095 Package: outer package [10 Units] In Commercial Distribution |
| FGY | Cannula, Injection |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2023-05-19 |
| Device Publish Date | 2023-02-06 |
| 06971162816881 | Y type |
| 06971162816874 | Y type |
| 06971162816867 | Y type |
| 06971162816850 | Y type |
| 06971162816843 | Y type |
| 06971162812234 | 18G |
| 06971162812227 | 20G |
| 06971162812210 | 22G |
| 06971162812203 | 24G |
| 06971162812197 | 26G |
| 06936841208098 | II-B-18G |