| Primary Device ID | 16959664900014 |
| NIH Device Record Key | e8559fc0-a69b-4013-9624-a2daa4e2b1c4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NA |
| Version Model Number | AG-5041-2526 |
| Company DUNS | 542984702 |
| Company Name | Hangzhou AGS MedTech 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06959664900017 [Primary] |
| GS1 | 16959664900014 [Package] Contains: 06959664900017 Package: box [10 Units] In Commercial Distribution |
| GS1 | 26959664900011 [Package] Package: carton [100 Units] In Commercial Distribution |
| OCY | Endoscopic Guidewire, Gastroenterology-Urology |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-10-17 |
| Device Publish Date | 2022-10-09 |
| 16959664912123 | AG-5099-05 |
| 16959664912055 | AG-5098-0525 |
| 16959664900830 | AG-5063-S2524G |
| 16959664900786 | AG-5062-N3024G |
| 16959664900779 | AG-5062-N2524G |
| 16959664900762 | AG-5062-N2024G |
| 16959664900106 | AG-5041-2526 |
| 16959664900021 | AG-5041-3526 |
| 16959664900014 | AG-5041-2526 |