Nebulizer Compressor Filter

GUDID 10709078005586

Nebulizer Compressor Filter

WESTMED, INC.

Heat/moisture exchanger/microbial filter, non-sterile Heat/moisture exchanger/microbial filter, non-sterile Heat/moisture exchanger/microbial medical gas filter Heat/moisture exchanger/microbial medical gas filter Heat/moisture exchanger/microbial medical gas filter Heat/moisture exchanger/microbial medical gas filter Heat/moisture exchanger/microbial medical gas filter Heat/moisture exchanger/microbial medical gas filter Heat/moisture exchanger/microbial medical gas filter Heat/moisture exchanger/microbial medical gas filter Heat/moisture exchanger/microbial medical gas filter Heat/moisture exchanger/microbial medical gas filter Heat/moisture exchanger/microbial medical gas filter Heat/moisture exchanger/microbial medical gas filter Heat/moisture exchanger/microbial medical gas filter Heat/moisture exchanger/microbial medical gas filter
Primary Device ID10709078005586
NIH Device Record Keybf3187e5-27e3-4dc9-8ff7-2ca6cbcd3237
Commercial Distribution StatusIn Commercial Distribution
Brand NameNebulizer Compressor Filter
Version Model Number6313
Company DUNS092673953
Company NameWESTMED, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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 Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100709078005589 [Primary]
GS110709078005586 [Package]
Contains: 00709078005589
Package: [4 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

CAHFilter, Bacterial, Breathing-Circuit

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-07-02
Device Publish Date2018-05-16

Devices Manufactured by WESTMED, INC.

20889483612009 - Anesthesia Circuit Kit 2024-06-10 60" Adult Anesthesia Circuit; Swivel Wye, 2L LF Bag
20889483612016 - Anesthesia Circuit Kit 2024-06-10 60" Adult Anes. Circuit; Par-Wye, GSE, 2L Latex Free
20889483612023 - Anesthesia Circuit Kit 2024-06-10 60" Pediatric Anes. Circuit, Par-Wye, GSE W/Port
20889483612030 - Anesthesia Circuit Kit 2024-06-10 UniLim,120" Adult.Coa.Circuit,Elbow,24Flex Expiratory
20889483612047 - Anesthesia Circuit Kit 2024-06-10 UniLim,72" Adult.Coa.Cir,GSE,24Flex Expiratory
20889483612054 - Anesthesia Circuit Kit 2024-06-10 96" Adult Exp.Anes.Circuit,Par-Wye,GSE W/Cap
20889483612061 - Anesthesia Circuit Kit 2024-06-10 72" ,Adult Anes.Circuit,Bi-Wye,Elbow 2L/Lf Bag
20889483612078 - Anesthesia Circuit Kit 2024-06-10 60" Adult Anes.Circuit,Par-Wye,GSE, No Bag

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.