MERGE EYE STATION 11.4

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2016-02-12 for MERGE EYE STATION 11.4 manufactured by Merge Healthcare.

Event Text Entries

[38210579] Merge eye station is intended to be used in conjunction with existing ophthalmic fundus cameras to take images of the eye, perform fluorescein angiography, red free, color and icg still-image photography as well as video imaging. On (b)(6) 2016 merge healthcare was notified that this customer's eyestation was not able to capture images. As a result of the malfunction, the customer was not able to scan patients for over 24 hours, which could potentially lead to a delay in diagnosis or treatment. The product is now functioning as expected because merge healthcare was able to send the customer replacement computer hardware.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2183926-2016-00446
MDR Report Key5435588
Report SourceUSER FACILITY
Date Received2016-02-12
Date of Report2016-02-12
Date of Event2016-01-13
Date Mfgr Received2016-01-13
Date Added to Maude2016-02-12
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. MICHAEL DIEDRICK
Manufacturer Street900 WALNUT RIDGE DRIVE
Manufacturer CityHARTLAND WI 53029
Manufacturer CountryUS
Manufacturer Postal53029
Manufacturer Phone2629123570
Manufacturer G1MERGE HEALTHCARE
Manufacturer Street900 WALNUT RIDGE DRIVE
Manufacturer CityHARTLAND WI 53029
Manufacturer CountryUS
Manufacturer Postal Code53029
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMERGE EYE STATION
Generic NameCAMERA, OPHTHALMIC, AC-POWERED
Product CodeNFJ
Date Received2016-02-12
Model NumberMERGE EYE STATION
Catalog Number11.4
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerMERGE HEALTHCARE
Manufacturer Address900 WALNUT RIDGE DRIVE HARTLAND WI 53029 US 53029


Patients

Patient NumberTreatmentOutcomeDate
10 2016-02-12

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