VISION FP 202

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 00 report with the FDA on 2001-02-02 for VISION FP 202 manufactured by Smv International.

Event Text Entries

[214517] After interfile report operation from vision for static images, the user can't display image because image duration time is always equal zero.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9615727-2001-00003
MDR Report Key315437
Report Source00
Date Received2001-02-02
Date of Report2001-02-02
Date of Event2001-01-24
Date Mfgr Received2001-01-24
Date Added to Maude2001-02-13
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location0
Manufacturer ContactMARCO TIRELLI
Manufacturer Street105 AV. MORANE-SAULNIER
Manufacturer CityBUC CEDEX 78534
Manufacturer CountryFR
Manufacturer Postal78534
Manufacturer Phone0849100
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Removal Correction NumberUNK
Event Type3
Type of Report3

Device Details

Brand NameVISION
Generic NameCOMPUTER
Product CodeJWM
Date Received2001-02-02
Model NumberVISION
Catalog NumberFP 202
Lot NumberNA
ID NumberNA
OperatorOTHER
Device AvailabilityY
Device Eval'ed by MfgrY
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key305034
ManufacturerSMV INTERNATIONAL
Manufacturer Address105 AV. MORANE-SAULNIER BUC CEDEX FR 78534
Baseline Brand NameVISION
Baseline Generic NameCOMPUTER
Baseline Model NoVISION
Baseline Catalog NoFP 202
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
10 2001-02-02

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