GAS MODULE

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06,07 report with the FDA on 2015-05-29 for GAS MODULE manufactured by Mindray Bio-med Electronics Co. Ltd..

Event Text Entries

[5925835] Customer reported an issue with the gas module which may have affected patient monitoring. No patient injury was reported.
Patient Sequence No: 1, Text Type: D, B5


[13283688] The device was evaluated. Corrections included calibrating the gas module. Performance tested to factory specifications.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2221819-2015-00233
MDR Report Key4810958
Report Source05,06,07
Date Received2015-05-29
Date of Report2015-04-14
Date of Event2015-03-24
Date Facility Aware2015-04-14
Report Date2015-04-14
Date Mfgr Received2015-04-14
Date Added to Maude2015-06-25
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactPATRICE SORIANO
Manufacturer Street800 MACARTHUR BLVD.
Manufacturer CityMAHWAH NJ 07430
Manufacturer CountryUS
Manufacturer Postal07430
Manufacturer Phone2019958026
Manufacturer G1MINDRAY BIO-MED ELECTRONICS CO. LTD.
Manufacturer StreetKEJI 12TH ROAD SOUTH NANSHAN
Manufacturer CitySHENZHEN 518057
Manufacturer CountryCH
Manufacturer Postal Code518057
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameGAS MODULE
Generic NameGAS MODULE
Product CodeBZK
Date Received2015-05-29
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerMINDRAY BIO-MED ELECTRONICS CO. LTD.
Manufacturer AddressNASHAN SHENZHEN CH


Patients

Patient NumberTreatmentOutcomeDate
10 2015-05-29

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