Bear Compressor Nebulizer

GUDID 00616784560939

DYNAREX CORPORATION

Nebulizing system, non-heated
Primary Device ID00616784560939
NIH Device Record Key77c5ccb5-cc0e-42be-9f04-d411d9d921a0
Commercial Distribution StatusIn Commercial Distribution
Brand NameBear Compressor Nebulizer
Version Model Number5609
Company DUNS008124539
Company NameDYNAREX CORPORATION
Device Count6
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numbertrue
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
GS100616784560915 [Unit of Use]
GS100616784560939 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

CAFNebulizer (Direct Patient Interface)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-05-29
Device Publish Date2019-05-21

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