| Primary Device ID | 08800196100803 |
| NIH Device Record Key | 92809551-4f4e-4792-81a5-27b2de2f9762 |
| Commercial Distribution Discontinuation | 2024-01-26 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Husteon MeshNasal |
| Version Model Number | HMNSS050-4010 |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08800196100803 [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 | 2024-02-05 |
| Device Publish Date | 2024-01-26 |
| 08800196110185 | HMNSS100-4010 |
| 08800196110178 | HMNSS080-4010 |
| 08800196110161 | HMNSS050-4010 |
| 08800196110154 | HMNSS100-3010 |
| 08800196110147 | HMNSS080-3010 |
| 08800196110130 | HMNSS050-3010 |
| 08800196110123 | HMNS100-4010 |
| 08800196110116 | HMNS080-4010 |
| 08800196110109 | HMNS050-4010 |
| 08800196110093 | HMNS100-3010 |
| 08800196110086 | HMNS080-3010 |
| 08800196110079 | HMNS050-3010 |
| 08800196110062 | HMN100-4010 |
| 08800196110055 | HMN080-4010 |
| 08800196110048 | HMN050-4010 |
| 08800196110031 | HMN100-3010 |
| 08800196110024 | HMN080-3010 |
| 08800196110017 | HMN050-3010 |
| 08800196110000 | HMN015-2015 |
| 08800196100803 | HMNSS050-4010 |