| Primary Device ID | 08800196100575 |
| NIH Device Record Key | 551100ee-8d18-46c7-88f5-893190a9e46a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Husteon Nasal |
| Version Model Number | HNS100-4010 |
| Company DUNS | 694603020 |
| Company Name | MediFab 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 | false |
| 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 | 08800196100575 [Primary] |
| LYA | Splint, Intranasal Septal |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-07-11 |
| Device Publish Date | 2022-07-01 |
| 08800196100636 | HNSS100-4010 |
| 08800196100629 | HNSS080-4010 |
| 08800196100612 | HNSS050-4010 |
| 08800196100605 | HNSS100-3010 |
| 08800196100599 | HNSS080-3010 |
| 08800196100582 | HNSS050-3010 |
| 08800196100575 | HNS100-4010 |
| 08800196100568 | HNS080-4010 |
| 08800196100551 | HNS050-4010 |
| 08800196100544 | HNS100-3010 |
| 08800196100537 | HNS080-3010 |
| 08800196100520 | HNS050-3010 |
| 08800196100513 | HN100-4010 |
| 08800196100506 | HN080-4010 |
| 08800196100490 | HN050-4010 |
| 08800196100483 | HN100-3010 |
| 08800196100476 | HN080-3010 |
| 08800196100469 | HN050-3010 |