FDA Adverse Event Malfunction Summary report: N

AS3000 ANESTHESIA SYSTEM

MDR report key: 3091325 · Received April 30, 2013

Report

Report Number
2221819-2013-00188
Event Type
Malfunction
Date Received
April 30, 2013
Date of Event
September 18, 2012
Report Date
April 30, 2013
Manufacturer
MINDRAY DS USA, INC.
Product Code
BSZ
PMA / PMN Number
080175
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WV, US
Reporter Occupation
UNKNOWN

Narratives

Description of Event or Problem · 1

CUSTOMER REPORTED A SYSTEM LEAK ON THE AS3000 ANESTHESIA SYSTEM. NO PATIENT INJURY WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
187302 AS3000 ANESTHESIA SYSTEM ANESTHESIA DELIVERY SYSTEM BSZ MINDRAY DS USA, INC.

Patients

Seq Age Sex Outcome Treatment
1