DISSOLUTION UNIT-TESTED DRY ACID MIXER- GRAN G047-80101

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2019-08-06 for DISSOLUTION UNIT-TESTED DRY ACID MIXER- GRAN G047-80101 manufactured by Concord Manufacturing.

MAUDE Entry Details

Report Number2937457-2019-02436
MDR Report Key8865390
Report SourceUSER FACILITY
Date Received2019-08-06
Date of Report2019-08-15
Date of Event2019-07-18
Date Mfgr Received2019-08-09
Device Manufacturer Date2003-05-07
Date Added to Maude2019-08-06
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationBIOMEDICAL ENGINEER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMATTHEW AMARAL
Manufacturer Street920 WINTER ST.
Manufacturer CityWALTHAM MA 02451
Manufacturer CountryUS
Manufacturer Postal02451
Manufacturer Phone7816999758
Manufacturer G1CONCORD MANUFACTURING
Manufacturer StreetDIRECTOR, QUALITY SYSTEMS 4040 NELSON AVENUE
Manufacturer CityCONCORD CA 94520
Manufacturer CountryUS
Manufacturer Postal Code94520
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameDISSOLUTION UNIT-TESTED
Generic NameBLENDER/MIXER
Product CodeJRO
Date Received2019-08-06
Model NumberDRY ACID MIXER- GRAN
Catalog NumberG047-80101
Lot NumberN/A
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeMO
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCONCORD MANUFACTURING
Manufacturer Address4040 NELSON AVENUE CONCORD CA 94520 US 94520


Patients

Patient NumberTreatmentOutcomeDate
10 2019-08-06

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