Husteon Nasal

GUDID 08800196100469

MediFab Co., Ltd

Intranasal splint, biodegradable
Primary Device ID08800196100469
NIH Device Record Key688957ff-d2d4-4dbd-8eef-fb39a799aa6c
Commercial Distribution StatusIn Commercial Distribution
Brand NameHusteon Nasal
Version Model NumberHN050-3010
Company DUNS694603020
Company NameMediFab Co., Ltd
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108800196100469 [Primary]

FDA Product Code

LYASplint, Intranasal Septal

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-07-11
Device Publish Date2022-07-01

On-Brand Devices [Husteon Nasal]

08800196100636HNSS100-4010
08800196100629HNSS080-4010
08800196100612HNSS050-4010
08800196100605HNSS100-3010
08800196100599HNSS080-3010
08800196100582HNSS050-3010
08800196100575HNS100-4010
08800196100568HNS080-4010
08800196100551HNS050-4010
08800196100544HNS100-3010
08800196100537HNS080-3010
08800196100520HNS050-3010
08800196100513HN100-4010
08800196100506HN080-4010
08800196100490HN050-4010
08800196100483HN100-3010
08800196100476HN080-3010
08800196100469HN050-3010

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