| Primary Device ID | 08800038405325 |
| NIH Device Record Key | 65b30fc4-23af-4dcc-b48f-d8643911e313 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Nexpowder |
| Version Model Number | NHS01 |
| Company DUNS | 689845781 |
| Company Name | NEXTBIOMEDICAL CO., LTD. |
| 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 | true |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | false |
| 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 | 08800038405325 [Primary] |
| GS1 | 18800038405322 [Package] Package: Box [5 Units] In Commercial Distribution |
| GS1 | 28800038405329 [Package] Contains: 18800038405322 Package: 90 [5 Units] In Commercial Distribution |
| QAU | Hemostatic Device For Endoscopic Gastrointestinal Use |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-10-13 |
| Device Publish Date | 2023-10-05 |
| 18800038405186 | Nexpowder is used for hemostasis of non-variceal, upper gastrointestinal bleeding. |
| 08800038405332 | Nexpowder is used for hemostasis of non-variceal, upper gastrointestinal bleeding. |
| 08800038405325 | expowder is used for hemostasis of non-variceal, upper gastrointestinal bleeding. |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() NEXPOWDER 79295194 not registered Live/Pending |
NEXTBIOMEDICAL CO., LTD. 2020-08-27 |
![]() NEXPOWDER 79283530 not registered Live/Pending |
NEXTBIOMEDICAL CO., LTD. 2020-03-18 |