| Primary Device ID | 16959664900854 |
| NIH Device Record Key | 094f0c9a-2ab0-4238-b630-2b1080868ea5 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | AG-5102-2300-090 |
| Company DUNS | 542984702 |
| Company Name | Hangzhou AGS MedTech Co., Ltd. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06959664900857 [Primary] |
| GS1 | 16959664900854 [Package] Contains: 06959664900857 Package: box [10 Units] In Commercial Distribution |
| GS1 | 26959664900851 [Package] Package: carton [10 Units] In Commercial Distribution |
| PKL | Hemostatic Metal Clip For The Gi Tract |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-12-12 |
| Device Publish Date | 2025-12-04 |
| 16959664900366 - NA | 2025-12-12 |
| 16959664900373 - NA | 2025-12-12 |
| 16959664900854 - NA | 2025-12-12 |
| 16959664900854 - NA | 2025-12-12 |
| 16959664903053 - NA | 2025-12-12 |
| 16959664903060 - NA | 2025-12-12 |
| 16959664903084 - NA | 2025-12-12 |
| 16959664903091 - NA | 2025-12-12 |
| 16959664903114 - NA | 2025-12-12 |