IOLMASTER 700 N/A 000003-5773-490

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2018-11-02 for IOLMASTER 700 N/A 000003-5773-490 manufactured by Carl Zeiss Meditec Ag (jena).

Event Text Entries

[125975720] The hcp did not allege a device malfunction and declined a device evaluation by czmi. The hcp added that the calculation from the iolmaster was perfect and the lens power was correct. The decentralized lens occured due to a weak zunula or a weak capsular, which he did not detect intra-operatively.
Patient Sequence No: 1, Text Type: N, H10


[125975721] A health care professional (hcp) reported that he used the iolmaster 700 for the biometry measurements and lens power calculations for a patient. After implanting the iol, one week post operatively, he found that the lens was decentered. The patient had dysopsia and poor visual acuity. The hcp performed a lens exchange to correct the patient's vision.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9615030-2018-00011
MDR Report Key8033796
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2018-11-02
Date of Report2018-10-05
Date Mfgr Received2018-10-05
Device Manufacturer Date2016-12-20
Date Added to Maude2018-11-02
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. VERNON BROWN
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 7745
Manufacturer CountryGM
Manufacturer Postal Code7745
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameIOLMASTER 700
Generic NameBIOMICROSCOPE, SLIT-LAMP, AC-POWERED
Product CodeHJO
Date Received2018-11-02
Model NumberN/A
Catalog Number000003-5773-490
Lot NumberN/A
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerCARL ZEISS MEDITEC AG (JENA)
Manufacturer AddressCARL ZEISS PROMENADE 10 JENA, THUERINGIA 7745 GM 7745


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2018-11-02

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.