FDA Adverse Event Injury Summary report: N

ELLMAN SURGITRON EMC

MDR report key: 213194 · Received March 10, 1999

Report

Report Number
2428235-1999-00001
Event Type
Injury
Date Received
March 10, 1999
Date of Event
December 5, 1998
Report Date
March 8, 1999
Manufacturer
ELLMAN INTERNATIONAL, INC.
Product Code
GEI
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
PHYSICIAN

Narratives

Description of Event or Problem · 1

SUPERFICIAL LEFT CORNEAL LACERATION DURING BLEPHAROPLASTY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ELLMAN SURGITRON EMC RADIOSURGERY GENERATOR GEI ELLMAN INTERNATIONAL, INC. EMC *

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN Other