CDI™ Shunt Sensor

GUDID 50699753160762

Terumo Cardiovascular Systems Corporation

Cardiopulmonary bypass system blood gas sensor Cardiopulmonary bypass system blood gas sensor
Primary Device ID50699753160762
NIH Device Record Key4a646dfb-f506-41d0-aa0c-5d1864b99a2a
Commercial Distribution StatusIn Commercial Distribution
Brand NameCDI™ Shunt Sensor
Version Model NumberCDI510H
Company DUNS177655466
Company NameTerumo Cardiovascular Systems Corporation
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 Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100699753160767 [Primary]
GS150699753160762 [Package]
Contains: 00699753160767
Package: 20 Piece Case [20 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DRYMonitor, Blood-Gas, On-Line, 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 Date2016-10-06

Devices Manufactured by Terumo Cardiovascular Systems Corporation

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00699753531406 - Cardiovascular Procedure Kit2024-05-20
00699753531413 - Cardiovascular Procedure Kit2024-05-20
00699753531420 - Cardiovascular Procedure Kit2024-05-20
00699753531338 - Cardiovascular Procedure Kit2024-05-17
00699753531345 - Cardiovascular Procedure Kit2024-05-17
00699753531352 - Cardiovascular Procedure Kit2024-05-17
00699753531369 - Cardiovascular Procedure Kit2024-05-17

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