enableCV Dual Stage Venous Drainage Cannula

GUDID 00840479400310

enableCV Dual Stage Venous Drainage Cannula - TR3240L

ENABLECV INC.

Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, drainage
Primary Device ID00840479400310
NIH Device Record Keya6b3ed60-2127-412e-a7d4-136c0e536516
Commercial Distribution StatusIn Commercial Distribution
Brand NameenableCV Dual Stage Venous Drainage Cannula
Version Model NumberTR3240L
Company DUNS119247843
Company NameENABLECV 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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1(888)943-2783
Emailcustomerservice@enablecv.com
Phone1(888)943-2783
Emailcustomerservice@enablecv.com
Phone1(888)943-2783
Emailcustomerservice@enablecv.com
Phone1(888)943-2783
Emailcustomerservice@enablecv.com
Phone1(888)943-2783
Emailcustomerservice@enablecv.com
Phone1(888)943-2783
Emailcustomerservice@enablecv.com
Phone1(888)943-2783
Emailcustomerservice@enablecv.com
Phone1(888)943-2783
Emailcustomerservice@enablecv.com
Phone1(888)943-2783
Emailcustomerservice@enablecv.com
Phone1(888)943-2783
Emailcustomerservice@enablecv.com
Phone1(888)943-2783
Emailcustomerservice@enablecv.com
Phone1(888)943-2783
Emailcustomerservice@enablecv.com

Device Dimensions

Device Size Text, specify0
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Device Size Text, specify0
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Device Size Text, specify0
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Device Size Text, specify0

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Store sterile packaged device in a cool, dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store sterile packaged device in a cool, dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store sterile packaged device in a cool, dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store sterile packaged device in a cool, dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store sterile packaged device in a cool, dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store sterile packaged device in a cool, dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store sterile packaged device in a cool, dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store sterile packaged device in a cool, dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store sterile packaged device in a cool, dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store sterile packaged device in a cool, dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store sterile packaged device in a cool, dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store sterile packaged device in a cool, dry place.

Device Identifiers

Device Issuing AgencyDevice ID
GS100840479400303 [Primary]
GS100840479400310 [Package]
Contains: 00840479400303
Package: [10 Units]
In Commercial Distribution

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 Date2026-02-23
Device Publish Date2026-02-14

On-Brand Devices [enableCV Dual Stage Venous Drainage Cannula]

00840479400310enableCV Dual Stage Venous Drainage Cannula - TR3240L
00840479400297enableCV Dual Stage Venous Drainage Cannula - TR3240O
00840479400273enableCV Dual Stage Venous Drainage Cannula - TR3240OA
00840479400259enableCV Dual Stage Venous Drainage Cannula - TR3446L

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