VERION DIGITAL MARKER M X-SPM 8065998244

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-01-17 for VERION DIGITAL MARKER M X-SPM 8065998244 manufactured by Wavelight Gmbh (agps).

Event Text Entries

[133839129] Investigation, including root cause analysis, is in progress. A supplemental mdr will be filed as necessary in accordance with 21 cfr 803. 56 when additional reportable information becomes available. (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[133839130] A surgeon reported a flickering phenomenon during a procedure. The surgeon noted that he does not use the diagnostic tool anymore since the visible line designating the axis was flickering/changing by about 20 degrees. One second it would be there and the next it would be completely at a different axis. Surgeon feels that the system is possessed and is not sure what the correct axis is on some cases. All of the intraocular lens were off a little. They were all toric lenses (t2's) and it has not impacted outcomes much. The exact number of patients involved is unknown. Additional information has been requested.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3010300699-2019-00001
MDR Report Key8256312
Date Received2019-01-17
Date of Report2019-02-14
Date of Event2018-12-10
Date Mfgr Received2019-02-11
Date Added to Maude2019-01-17
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 ContactMS. CINDY MILAM
Manufacturer Street6201 SOUTH FREEWAY MAIL STOP AB2-6
Manufacturer CityFORT WORTH TX 76134
Manufacturer CountryUS
Manufacturer Postal76134
Manufacturer Phone8176152231
Manufacturer G1WAVELIGHT GMBH (AGPS)
Manufacturer StreetRHEINSTRASSE 8
Manufacturer CityTELTOW 14513
Manufacturer CountryGM
Manufacturer Postal Code14513
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report0

Device Details

Brand NameVERION DIGITAL MARKER M
Generic NameMARKER, OCULAR
Product CodeFTH
Date Received2019-01-17
Model NumberX-SPM
Catalog Number8065998244
Lot NumberASKU
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerWAVELIGHT GMBH (AGPS)
Manufacturer AddressRHEINSTRASSE 8 TELTOW 14513 GM 14513


Patients

Patient NumberTreatmentOutcomeDate
10 2019-01-17

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