Fem-Flex II Femoral Arterial Cannula FEMII018AS

GUDID 00690103168358

FEM-FLEX II Femoral Arterial Cannula

Edwards Lifesciences LLC

Cardiopulmonary bypass cannula, femoral Cardiopulmonary bypass cannula, femoral Cardiopulmonary bypass cannula, venous Cardiopulmonary bypass cannula, venous Cardiopulmonary bypass cannula, venous Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, venous Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, venous Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, venous Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, venous Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, venous Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, venous Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, venous Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, venous Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, venous Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, venous Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, venous
Primary Device ID00690103168358
NIH Device Record Keyf5396ce5-fe71-46f4-804a-4ef9126c7725
Commercial Distribution StatusIn Commercial Distribution
Brand NameFem-Flex II Femoral Arterial Cannula
Version Model NumberFEMII018AS
Catalog NumberFEMII018AS
Company DUNS134139174
Company NameEdwards Lifesciences 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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)822-9637
Emailtech_support@edwards.com
Phone+1(800)822-9637
Emailtech_support@edwards.com
Phone+1(800)822-9637
Emailtech_support@edwards.com
Phone+1(800)822-9637
Emailtech_support@edwards.com
Phone+1(800)822-9637
Emailtech_support@edwards.com
Phone+1(800)822-9637
Emailtech_support@edwards.com
Phone+1(800)822-9637
Emailtech_support@edwards.com
Phone+1(800)822-9637
Emailtech_support@edwards.com
Phone+1(800)822-9637
Emailtech_support@edwards.com
Phone+1(800)822-9637
Emailtech_support@edwards.com
Phone+1(800)822-9637
Emailtech_support@edwards.com
Phone+1(800)822-9637
Emailtech_support@edwards.com
Phone+1(800)822-9637
Emailtech_support@edwards.com
Phone+1(800)822-9637
Emailtech_support@edwards.com
Phone+1(800)822-9637
Emailtech_support@edwards.com
Phone+1(800)822-9637
Emailtech_support@edwards.com

Device Dimensions

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Device Identifiers

Device Issuing AgencyDevice ID
GS100690103168358 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DWFCATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-08-31

On-Brand Devices [Fem-Flex II Femoral Arterial Cannula]

00690103168365FEM-FLEX II Femoral Arterial Cannula
00690103168358FEM-FLEX II Femoral Arterial Cannula
00690103168341FEM-FLEX II Femoral Arterial Cannula
00690103031287FEM-FLEX II Femoral Arterial Cannula
00690103031256FEM-FLEX II Femoral Arterial Cannula
00690103031232FEM-FLEX II Femoral Arterial Cannula
00690103031195FEM-FLEX II Femoral Arterial Cannula
00690103031171FEM-FLEX II Femoral Arterial Cannula
00690103031133FEM-FLEX II Femoral Arterial Cannula
00690103031119FEM-FLEX II Femoral Arterial Cannula
00690103031072FEM-FLEX II Femoral Arterial Cannula
00690103031058FEM-FLEX II Femoral Arterial Cannula
00690103031010FEM-FLEX II Femoral Arterial Cannula
00690103030990FEM-FLEX II Femoral Arterial Cannula

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