B&F

GUDID 00260720011223

Humidifier

ALLIED HEALTHCARE PRODUCTS, INC.

Non-heated respiratory humidifier
Primary Device ID00260720011223
NIH Device Record Keyaab0f3a7-b245-4add-b8bf-d20cd5883b30
Commercial Distribution StatusIn Commercial Distribution
Brand NameB&F
Version Model Number64375
Company DUNS099674145
Company NameALLIED HEALTHCARE PRODUCTS, INC.
Device Count50
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 Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100260720011223 [Primary]
GS140260720011221 [Unit of Use]

FDA Product Code

BTTHumidifier, Respiratory Gas, (Direct Patient Interface)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-08-24

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00260720011186Nebulizer Kit
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00260720011131Nebulizer
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00260720011117Nebulizer Kit
00260720011100Nebulizer Set
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00260720011087Nebulizer Kit
00260720011070Nebulizer Kit
00026072011256Humidifier
00026072011249Humidifier
00026072011232Humidifier
00026072011225Humidifier
00026072011218Mask, Ped Aerosol Neb
00026072011188Nebulizer Kit
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00026072011126Nebulizer
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00026072011102Nebulizer Set
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