AVX 105039

GUDID 00616258003832

AVX CUS CATHETER, FG PKG

Bayer Healthcare LLC

Thrombectomy suction catheter
Primary Device ID00616258003832
NIH Device Record Keyb2964cfc-0eb1-4f6b-b46f-fcd0ee4624b8
Commercial Distribution StatusIn Commercial Distribution
Brand NameAVX
Version Model Number105039-001
Catalog Number105039
Company DUNS079415074
Company NameBayer Healthcare LLC
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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone763-780-4555
Emailmichael.burnside@bayer.com
Phone763-780-4555
Emailmichael.burnside@bayer.com
Phone763-780-4555
Emailmichael.burnside@bayer.com
Phone763-780-4555
Emailmichael.burnside@bayer.com
Phone763-780-4555
Emailmichael.burnside@bayer.com
Phone763-780-4555
Emailmichael.burnside@bayer.com
Phone763-780-4555
Emailmichael.burnside@bayer.com
Phone763-780-4555
Emailmichael.burnside@bayer.com
Phone763-780-4555
Emailmichael.burnside@bayer.com
Phone763-780-4555
Emailmichael.burnside@bayer.com
Phone763-780-4555
Emailmichael.burnside@bayer.com
Phone763-780-4555
Emailmichael.burnside@bayer.com
Phone763-780-4555
Emailmichael.burnside@bayer.com

Device Dimensions

Catheter Gauge6 French
Catheter Gauge6 French
Catheter Gauge6 French
Catheter Gauge6 French
Catheter Gauge6 French
Catheter Gauge6 French
Catheter Gauge6 French
Catheter Gauge6 French
Catheter Gauge6 French
Catheter Gauge6 French
Catheter Gauge6 French
Catheter Gauge6 French
Catheter Gauge6 French

Device Identifiers

Device Issuing AgencyDevice ID
GS100616258003832 [Primary]

FDA Product Code

DXECatheter, Embolectomy

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2014-10-09

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