Primary Device ID | 08800196100469 |
NIH Device Record Key | 688957ff-d2d4-4dbd-8eef-fb39a799aa6c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Husteon Nasal |
Version Model Number | HN050-3010 |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08800196100469 [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 |