EOPA CAP™

GUDID 20613994888628

CANNULA 77918 EOPA CAP NONVENT 18FR

MEDTRONIC, INC.

Cardiopulmonary bypass cannula, arterial
Primary Device ID20613994888628
NIH Device Record Key77ea8f4a-f303-474c-9ff7-f2e664721c34
Commercial Distribution StatusIn Commercial Distribution
Brand NameEOPA CAP™
Version Model Number77918
Company DUNS006261481
Company NameMEDTRONIC, 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 Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com

Device Dimensions

Catheter Gauge18 French
Catheter Gauge18 French
Catheter Gauge18 French
Catheter Gauge18 French
Catheter Gauge18 French
Catheter Gauge18 French
Catheter Gauge18 French
Catheter Gauge18 French
Catheter Gauge18 French
Catheter Gauge18 French
Catheter Gauge18 French
Catheter Gauge18 French
Catheter Gauge18 French
Catheter Gauge18 French
Catheter Gauge18 French
Catheter Gauge18 French
Catheter Gauge18 French
Catheter Gauge18 French
Catheter Gauge18 French
Catheter Gauge18 French
Catheter Gauge18 French
Catheter Gauge18 French
Catheter Gauge18 French
Catheter Gauge18 French
Catheter Gauge18 French
Catheter Gauge18 French
Catheter Gauge18 French
Catheter Gauge18 French
Catheter Gauge18 French

Device Identifiers

Device Issuing AgencyDevice ID
GS120613994888628 [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 Date2017-01-22

On-Brand Devices [EOPA CAP™]

20643169486236CANNULA 77822 EOPA CAP 22FR 10PK 10L
20643169486229CANNULA 77820 EOPA CAP 20FR 10PK 10L
20643169486212CANNULA 77818 EOPA CAP 18FR 10PK 10L
20613994888642CANNULA 77922 EOPA CAP NONVENT 22FR
20613994888635CANNULA 77920 EOPA CAP NONVENT 20FR
20613994888628CANNULA 77918 EOPA CAP NONVENT 18FR

Trademark Results [EOPA CAP]

Mark Image

Registration | Serial
Company
Trademark
Application Date
EOPA CAP
EOPA CAP
78030450 2872461 Live/Registered
MEDTRONIC, INC.
2000-10-13

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