AIOBIO

GUDID 08800043200199

AIOBIO CO.,LTD

Mouth gag, adjustable, reusable
Primary Device ID08800043200199
NIH Device Record Key47655997-9863-4c5a-8ef3-60b56d227693
Commercial Distribution StatusIn Commercial Distribution
Brand NameAIOBIO
Version Model NumberW-Block
Company DUNS694894136
Company NameAIOBIO 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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108800043200199 [Primary]

FDA Product Code

KBNGag, Mouth

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-06-06
Device Publish Date2024-05-29

On-Brand Devices [AIOBIO]

08800043200199W-Block
08800043200069W-Block
08800043200038Qraypen
08800043200212LINKDENS VU

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