NeoBar Mini N709

GUDID 00812594011061

ET Tube Holder (Qty. 5)

NEOTECH PRODUCTS, INC.

Wearable percutaneous catheter/tube holder Wearable percutaneous catheter/tube holder Wearable percutaneous catheter/tube holder Wearable percutaneous catheter/tube holder Wearable percutaneous catheter/tube holder Wearable percutaneous catheter/tube holder Wearable percutaneous catheter/tube holder Wearable percutaneous catheter/tube holder Wearable percutaneous catheter/tube holder Wearable percutaneous catheter/tube holder Wearable percutaneous catheter/tube holder Wearable percutaneous catheter/tube holder Wearable percutaneous catheter/tube holder Wearable percutaneous catheter/tube holder Wearable percutaneous catheter/tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder
Primary Device ID00812594011061
NIH Device Record Key6ea886b8-5160-4d01-ad0d-2434dab2d3f3
Commercial Distribution StatusIn Commercial Distribution
Brand NameNeoBar Mini
Version Model Number10812594011068
Catalog NumberN709
Company DUNS198013435
Company NameNEOTECH PRODUCTS, INC.
Device Count5
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 Numbertrue
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100812594011061 [Unit of Use]
GS110812594011068 [Primary]

FDA Product Code

CBHDevice, Fixation, Tracheal Tube

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-06-10
Device Publish Date2021-06-02

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