Fem-Flex II Femoral Arterial Cannula FEMII020A

GUDID 00690103031287

FEM-FLEX II Femoral Arterial Cannula

Edwards Lifesciences LLC

Cardiopulmonary bypass cannula, venous Cardiopulmonary bypass cannula, venous 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 ID00690103031287
NIH Device Record Key4aeb52f5-be14-436b-bce9-27b842457eed
Commercial Distribution StatusIn Commercial Distribution
Brand NameFem-Flex II Femoral Arterial Cannula
Version Model NumberFEMII020A
Catalog NumberFEMII020A
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 Datetrue
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
GS100690103031287 [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 Number5
Public Version Date2020-06-29
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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