Cardiovascular Procedure Kit

GUDID 00699753533431

Terumo Cardiovascular Systems Corporation

Cardiopulmonary bypass system blood tubing set
Primary Device ID00699753533431
NIH Device Record Key69f01b47-00cd-400a-b0be-341a870e8695
Commercial Distribution StatusIn Commercial Distribution
Brand NameCardiovascular Procedure Kit
Version Model NumberCX-FR472X
Company DUNS177655466
Company NameTerumo Cardiovascular Systems Corporation
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latextrue
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100699753533431 [Primary]

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-11-21
Device Publish Date2024-11-13

On-Brand Devices [Cardiovascular Procedure Kit]

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5069975350975276970
5069975350973866743
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5069975350971476967
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0069975350930676838
5069975350929576820
5069975350928876906
5069975350927176904
5069975350926476901

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