Select Series™

GUDID 00643169696181

CANNULA CB72120 SELECT SERIES 20FR

MEDTRONIC, INC.

Cardiopulmonary bypass cannula, arterial Cardiopulmonary bypass cannula, arterial Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, arterial Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, arterial Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, arterial Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, arterial Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, arterial Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, arterial Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, arterial Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, arterial Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, arterial Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, arterial Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, arterial
Primary Device ID00643169696181
NIH Device Record Keyf7b25a0b-dc2e-49a2-a278-c71ce3998077
Commercial Distribution Discontinuation2017-08-25
Commercial Distribution StatusNot in Commercial Distribution
Brand NameSelect Series™
Version Model NumberCB72120
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 Producttrue
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

Device Dimensions

Catheter Gauge20 French
Catheter Gauge20 French
Catheter Gauge20 French
Catheter Gauge20 French
Catheter Gauge20 French
Catheter Gauge20 French
Catheter Gauge20 French
Catheter Gauge20 French
Catheter Gauge20 French
Catheter Gauge20 French
Catheter Gauge20 French
Catheter Gauge20 French
Catheter Gauge20 French

Operating and Storage Conditions

Storage Environment TemperatureBetween 0 Degrees Celsius and 40 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 40 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 40 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 40 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 40 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 40 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 40 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 40 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 40 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 40 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 40 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 40 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 40 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS100643169696181 [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 Date2017-03-04

On-Brand Devices [Select Series™]

00643169767881CANNULA CB72224 SEL SERIES ART 24FR 17L
00643169696204CANNULA CB72124 SELECT SERIES 24FR
00643169696198CANNULA CB72122 SEL SERIES ART 22FR
00643169696181CANNULA CB72120 SELECT SERIES 20FR
00643169560772CANN CB72124 SELECT ART STR 24F 17L
00763000192785CANNULA CB72224 SEL SERIES ART 24FR 17L
00763000192778CANN CB72124 SELECT ART STR 24F 17L

Trademark Results [Select Series]

Mark Image

Registration | Serial
Company
Trademark
Application Date
SELECT SERIES
SELECT SERIES
98433744 not registered Live/Pending
Strong Industries, Inc.
2024-03-05
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90548620 not registered Live/Pending
Culligan International Company
2021-02-26
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88925168 not registered Live/Pending
Waters Technologies Corporation
2020-05-20
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88826118 not registered Live/Pending
Waters Technologies Corporation
2020-03-09
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88217670 not registered Live/Pending
Waters Technologies Corporation
2018-12-05
SELECT SERIES
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87721369 5699487 Live/Registered
NutraClick, LLC
2017-12-14
SELECT SERIES
SELECT SERIES
85379013 4727894 Live/Registered
Sundance Spas, Inc.
2011-07-22
SELECT SERIES
SELECT SERIES
85140901 3969924 Live/Registered
Manna Pro Products, LLC
2010-09-29
SELECT SERIES
SELECT SERIES
78656768 3293587 Live/Registered
OMNIMAX INTERNATIONAL, INC.
2005-06-23
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SELECT SERIES
78413461 not registered Dead/Abandoned
Masonite Holdings, Inc.
2004-05-05
SELECT SERIES
SELECT SERIES
76451671 not registered Dead/Abandoned
Manna Pro Corporation
2002-09-20
SELECT SERIES
SELECT SERIES
76229141 not registered Dead/Abandoned
Colwell Merchandising, Inc.
2001-03-21

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