FDA Adverse Event Malfunction Summary report: N

MIRA OPHTHALMIC CRYO UNIT

MDR report key: 1910836 · Received November 23, 2010

Report

Report Number
1218813-2010-00014
Event Type
Malfunction
Date Received
November 23, 2010
Date of Event
June 4, 2010
Report Date
November 19, 2010
Manufacturer
MIRA, INC.
Product Code
GEH
PMA / PMN Number
K760686
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
NOT APPLICABLE

Narratives

Description of Event or Problem · 1

TUBING CONNECTING THE CRYO PROBE TO THE CRYO UNIT RUPTURED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MIRA OPHTHALMIC CRYO UNIT GEH MIRA, INC. CR4060

Patients

Seq Age Sex Outcome Treatment
1