EOPA™

GUDID 00763000946838

CANNULA 77624 EOPA DIL TIP 24FR 10PK 10L

MEDTRONIC, INC.

Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, return
Primary Device ID00763000946838
NIH Device Record Key9cd68c5b-9f59-421d-ade6-4700fbf318af
Commercial Distribution StatusIn Commercial Distribution
Brand NameEOPA™
Version Model Number77624
Company DUNS006261481
Company NameMEDTRONIC, INC.
Device Count10
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

Device Dimensions

Catheter Gauge24 French
Catheter Gauge24 French
Catheter Gauge24 French
Catheter Gauge24 French
Catheter Gauge24 French
Catheter Gauge24 French
Catheter Gauge24 French
Catheter Gauge24 French
Catheter Gauge24 French
Catheter Gauge24 French
Catheter Gauge24 French
Catheter Gauge24 French
Catheter Gauge24 French
Catheter Gauge24 French
Catheter Gauge24 French
Catheter Gauge24 French

Device Identifiers

Device Issuing AgencyDevice ID
GS100763000946838 [Unit of Use]
GS120763000946832 [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 StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-11-04
Device Publish Date2024-10-27

On-Brand Devices [EOPA™]

00643169696143CANNULA CB77724 EOPA DIL TIP 24FR
00643169696136CANNULA CB77722 EOPA DIL TIP 22FR
00643169696129CANNULA CB77720 EOPA DIL TIP 20FR
00643169696112CANNULA CB77718 EOPA DIL TIP 18FR
00643169696105CANNULA CB77624 EOPA DIL TIP 24FR
00643169696099CANNULA CB77622 EOPA DIL 22FR
00643169696082CANNULA CB77620 EOPA DIL 20FR
00643169696075CANNULA CB77618 EOPA DIL 18FR
00643169696068CANNULA CB77524 EOPA BLUNT 24FR
00643169696051CANNULA CB77522 EOPA BLUNT 22FR
00643169696044CANNULA CB77520 EOPA BLUNT 20FR
00643169696037CANNULA CB77518 EOPA BLUNT 18FR
00643169696020CANNULA CB77424 EOPA BLUNT 24FR
00643169696013CANNULA CB77422 EOPA BLUNT 22FR
00643169696006CANNULA CB77420 EOPA BLUNT 20FR
00643169695993CANNULA CB77418 EOPA BLUNT 18FR
00643169561014CANN CB77622 EOPA DIL TIP VNTED 22FR 10L
00643169561007CANN CB77620 EOPA DIL TIP VNTED 20FR 10L
00643169560970CANN CB77422 EOPA BLUNT 22FR
00643169560963CANN CB77420 EOPA BLNT VEN 20F
20763000135687CANNULA 77624 EOPA DIL TIP 24FR 10PK 10L
20763000135670CANNULA 77622 EOPA DIL TIP 22FR 10PK 10L
20763000135663CANNULA 77620 EOPA DIL TIP 20FR 10PK 10L
20763000135656CANNULA 77618 EOPA DIL TIP 18FR 10PK 10L
20763000135649CANNULA 77424 EOPA BLUNT 24FR 10PK 11L
20763000135632CANNULA 77422 EOPA BLUNT 22FR 10PK 11L
20763000135625CANNULA 77420 EOPA BLUNT 20FR 10PK 11L
20763000135618CANNULA 77418 EOPA BLUNT 18FR 10PK 10L
20763000135601CANNULA 77724 EOPA DIL TIP NONVENT 24FR
20763000135595CANNULA 77722 EOPA DIL TIP NONVENT 22FR
20763000135588CANNULA 77720 EOPA DIL TIP NONVENT 20FR
20763000135571CANNULA 77718 EOPA DIL TIP NONVENT 18FR
20763000135564CANNULA 77524 EOPA BLUNT NONVENT 24FR
20763000135557CANNULA 77522 EOPA BLUNT NONVENT 22FR
20763000135540CANNULA 77520 EOPA BLUNT NONVENT 20FR
20763000135533CANNULA 77518 EOPA BLUNT NONVENT 18FR
20643169486205CANNULA 77624 EOPA DIL TIP 24FR 10PK 10L
20643169486199CANNULA 77622 EOPA DIL TIP 22FR 10PK 10L
20643169486182CANNULA 77620 EOPA DIL TIP 20FR 10PK 10L
20643169486175CANNULA 77618 EOPA DIL TIP 18FR 10PK 10L
20643169486168CANNULA 77424 EOPA BLUNT 24FR 10PK 11L
20643169486151CANNULA 77422 EOPA BLUNT 22FR 10PK 11L
20643169486144CANNULA 77420 EOPA BLUNT 20FR 10PK 11L
20643169486137CANNULA 77418 EOPA BLUNT 18FR 10PK 10L
20643169340491CANNULA 77724 EOPA DIL TIP NONVENT 24FR
20643169340484CANNULA 77722 EOPA DIL TIP NONVENT 22FR
20643169340477CANNULA 77720 EOPA DIL TIP NONVENT 20FR
20643169340460CANNULA 77718 EOPA DIL TIP NONVENT 18FR
20613994888833CANNULA 77524 EOPA BLUNT NONVENT 24FR
20613994888826CANNULA 77522 EOPA BLUNT NONVENT 22FR

Trademark Results [EOPA]

Mark Image

Registration | Serial
Company
Trademark
Application Date
EOPA
EOPA
78736242 3308983 Live/Registered
Medtronic, Inc.
2005-10-19
EOPA
EOPA
75606671 not registered Dead/Abandoned
Medtronic, Inc.
1998-12-16

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