Primary Device ID | 08800196110130 |
NIH Device Record Key | 99227362-dcce-4a6f-8b6f-7d10f0c75d60 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Husteon MeshNasal |
Version Model Number | HMNSS050-3010 |
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 | 08800196110130 [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 | 2023-03-02 |
Device Publish Date | 2023-02-22 |
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 |