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Labwindows Cvi Serial Number

Example of digital voltmeter with pic 16F688 microcontroller ADC reading and UART communication with CVI software through the serial port. I ask help please I am new to Labwindows and want to read hex values over the serial from a microcontroller, I use the functions below. Acquisition using LabView LabWindows/cvi Serial Communication with Arduino / Analog signal / Analog input / PWM How to Use IVI Specific and Class Drivers in LabWindows CVI NI LabWindows/CVI interface to Arduino UNO with LCD Shield LabWindows/CVI LabWindows/CVI - Interface - 3.1/n LabWindows/CVI DataSocket Tutorialการติดตั้ง NI.

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Labwindows Cvi Serial Number Lookup

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Labwindows Cvi Serial Numbers

ACIST MEDICAL SYSTEMS, INC. ACIST INJECTOR AND SYRINGE, ANGIOGRAPHICBack to Search Results
Model Number CVI
Device Problems Device Dislodged or Dislocated (2923); Adverse Event Without Identified Device or Use Problem (2993)
Patient Problem Vascular Dissection (3160)
Event Date 02/21/2019
Event Type Death
Manufacturer Narrative

Acist angiographic injection system, model cvi, serial number (b)(4) was received at acist on march 14, 2019. Investigation is in process. Upon completion of the investigation, acist will submit a followup report to fda.

Event Description

User facility reported, during a diagnostic catheterization of a patient with non-st-elevation myocardial infarction, upon injection of contrast media using the acist cvi injector, dissection of a patient's left internal mammary artery (lima) occurred. Upon the first selective shot, there was no dissection. The jr4 5fr catheter dislodged and could not re-engage. A non-selective shot revealed the lima dissection. The patient experienced chest pain, st-segment depression, hypotension, and myocardial infarction. The dissection was stented. The patient subsequently died the same day.

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Type of DeviceINJECTOR AND SYRINGE, ANGIOGRAPHIC
Manufacturer (Section D)
ACIST MEDICAL SYSTEMS, INC.
7905 fuller road
eden prairie MN 55344
Manufacturer (Section G)
ACIST MEDICAL SYSTEMS, INC.
7905 fuller road
eden prairie MN 55344
Manufacturer Contact
jeff audritsh
7905 fuller road
eden prairie, MN 55344
9529959347
MDR Report Key8467963
MDR Text Key140419305
Report Number2134243-2019-00004
Device Sequence Number1
Product Code DXT
Combination Product (Y/N)N
Reporter Country CodeUS
PMA/PMN NumberK010390
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source TypeHEALTH PROFESSIONAL,USER FACI
Reporter Occupation
Type of ReportInitial,Followup
Report Date03/18/2019
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received03/30/2019
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator HEALTH PROFESSIONAL
Device MODEL NumberCVI
Device Catalogue Number014657
Was Device Available For Evaluation? Device Returned To Manufacturer
Date Returned to Manufacturer03/14/2019
Is The Reporter A Health Professional? Yes
Was the Report Sent to FDA?
Event Location No Information
Date Manufacturer Received03/18/2019
Was Device Evaluated By Manufacturer? Yes
Date Device Manufactured09/14/2015
Is The Device Single Use? No
Is this a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Reuse

Patient TREATMENT DATA
Date Received: 03/30/2019 Patient Sequence Number: 1