IOLMASTER 700 000000-1932-169

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 2017-11-22 for IOLMASTER 700 000000-1932-169 manufactured by Carl Zeiss Meditec Ag (jena).

Event Text Entries

[92833488] A follow-up report will be submitted once the device evaluation is completed.
Patient Sequence No: 1, Text Type: N, H10


[92833489] The health care professional (hcp) reported the following: the od refractive outcome after cataract surgery with an intraocular lens (iol) implantation differed by 0. 50 diopter from the target refraction. The alcon acrysof iq restor iol sn6ad1 with a lens power of 19. 50 diopters was used. The hcp made a decision to exchange the iol. The iolmaster 700 was used for the original biometry measurements and lens power calculations.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9615030-2017-00025
MDR Report Key7054172
Report SourceUSER FACILITY
Date Received2017-11-22
Date of Report2017-10-27
Date of Event2017-10-18
Date Mfgr Received2017-10-27
Device Manufacturer Date2017-03-30
Date Added to Maude2017-11-22
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. WILLIAM GUSTAFSON
Manufacturer Street5160 HACIENDA DRIVE
Manufacturer CityDUBLIN CA 94568
Manufacturer CountryUS
Manufacturer Postal94568
Manufacturer Phone9255574689
Manufacturer G1CARL ZEISS MEDITEC AG (JENA)
Manufacturer StreetCARL ZEISS PROMENADE 10
Manufacturer CityJENA, THUERINGIA 07745
Manufacturer CountryGM
Manufacturer Postal Code07745
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameIOLMASTER 700
Generic NameBIOMICROSCOPE, SLIT-LAMP, AC-POWERED
Product CodeHJO
Date Received2017-11-22
Model NumberNA
Catalog Number000000-1932-169
Lot NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerCARL ZEISS MEDITEC AG (JENA)
Manufacturer AddressCARL ZEISS PROMENADE 10 JENA, THUERINGIA 07745 GM 07745


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2017-11-22

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