MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06,08 report with the FDA on 2014-12-10 for MALYUGIN RING SYSTEM MAL-0002-1 manufactured by Microsurgical Technology, Inc..
[5199661]
The user facility reported to the distributor that the malyugin ring tore a capsule when being inserted into the pupillary margin. The surgeon was able to salvage the capsular bag and implant and iol without further impact to the pt.
Patient Sequence No: 1, Text Type: D, B5
[12697261]
The eval on the returned device was inconclusive. The cause of the capsular tear is unk.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 3019924-2014-00056 |
MDR Report Key | 4346067 |
Report Source | 05,06,08 |
Date Received | 2014-12-10 |
Date of Report | 2014-12-05 |
Date Mfgr Received | 2014-11-11 |
Date Added to Maude | 2014-12-22 |
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 | 0 |
Event Location | 0 |
Manufacturer Street | 8415 154TH AVE., N.E. |
Manufacturer City | REDMOND WA 98052 |
Manufacturer Country | US |
Manufacturer Postal | 98052 |
Manufacturer Phone | 4255560544 |
Single Use | 3 |
Remedial Action | RL |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | MALYUGIN RING SYSTEM |
Generic Name | IRIS CLIP RETRACTOR |
Product Code | HOC |
Date Received | 2014-12-10 |
Returned To Mfg | 2014-11-26 |
Model Number | MAL-0002-1 |
Catalog Number | MAL-0002-1 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MICROSURGICAL TECHNOLOGY, INC. |
Manufacturer Address | REDMOND WA US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2014-12-10 |