| 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 |