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).
[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
Report Number | 9615030-2017-00025 |
MDR Report Key | 7054172 |
Report Source | USER FACILITY |
Date Received | 2017-11-22 |
Date of Report | 2017-10-27 |
Date of Event | 2017-10-18 |
Date Mfgr Received | 2017-10-27 |
Device Manufacturer Date | 2017-03-30 |
Date Added to Maude | 2017-11-22 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MR. WILLIAM GUSTAFSON |
Manufacturer Street | 5160 HACIENDA DRIVE |
Manufacturer City | DUBLIN CA 94568 |
Manufacturer Country | US |
Manufacturer Postal | 94568 |
Manufacturer Phone | 9255574689 |
Manufacturer G1 | CARL ZEISS MEDITEC AG (JENA) |
Manufacturer Street | CARL ZEISS PROMENADE 10 |
Manufacturer City | JENA, THUERINGIA 07745 |
Manufacturer Country | GM |
Manufacturer Postal Code | 07745 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | IOLMASTER 700 |
Generic Name | BIOMICROSCOPE, SLIT-LAMP, AC-POWERED |
Product Code | HJO |
Date Received | 2017-11-22 |
Model Number | NA |
Catalog Number | 000000-1932-169 |
Lot Number | NA |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | CARL ZEISS MEDITEC AG (JENA) |
Manufacturer Address | CARL ZEISS PROMENADE 10 JENA, THUERINGIA 07745 GM 07745 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2017-11-22 |