Cardiovascular Procedure Kit

GUDID 50699753532842

Terumo Cardiovascular Systems Corporation

Endoscopic-access dilator, single-use
Primary Device ID50699753532842
NIH Device Record Key9b24c2ad-b904-4cc8-87c8-aeff67b37a5e
Commercial Distribution StatusIn Commercial Distribution
Brand NameCardiovascular Procedure Kit
Version Model NumberCX-FR467
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
GS100699753532847 [Primary]
GS150699753532842 [Package]
Contains: 00699753532847
Package: 10 PIECE CASE [10 Units]
In Commercial Distribution

FDA Product Code

GCJLaparoscope, General & Plastic Surgery

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-09-19
Device Publish Date2024-09-11

On-Brand Devices [Cardiovascular Procedure Kit]

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5069975350976976969
5069975350975276970
5069975350973866743
0069975350972674109-01
5069975350971476967
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0069975350967276854
5069975350966076951
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5069975350952376869
5069975350951676903
0069975350950476922
5069975350949376939
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5069975350945576940
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00699753509412B75876-02
0069975350940576944
0069975350939972226-04
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5069975350937066653
5069975350936366652
5069975350935666651
5069975350934966650
0069975350933766649
0069975350932066648
0069975350931366647
0069975350930676838
5069975350929576820
5069975350928876906
5069975350927176904
5069975350926476901

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