ZM-920PA

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2019-07-02 for ZM-920PA manufactured by Nihon Kohden Corporation.

MAUDE Entry Details

Report Number8030229-2019-00264
MDR Report Key8755869
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2019-07-02
Date of Report2019-09-06
Date of Event2019-06-10
Date Facility Aware2019-09-05
Report Date2019-09-06
Date Reported to FDA2019-09-06
Date Reported to Mfgr2019-09-06
Date Mfgr Received2019-09-05
Device Manufacturer Date2004-06-21
Date Added to Maude2019-07-02
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 ContactSHAMA MOOMAN
Manufacturer StreetSAFETY MGMT DEPT, QUALITY MGMT SEIBU BLDG 2, 4TH FLOOR 1-11-2
Manufacturer CityKUSUNOKIDAI TOKOROZAWA, SAITAMA 359-8580
Manufacturer CountryJA
Manufacturer Postal359-8580
Manufacturer G1NIHON KOHDEN TOMIOKA CORPORATION
Manufacturer Street486 NANOKAICHI ATTN: SHAMA MOOMAN
Manufacturer CityTOMIOKA CITY, 370-2343
Manufacturer CountryJA
Manufacturer Postal Code370-2343
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameZM-920PA
Generic NameZM-920PA
Product CodeDRG
Date Received2019-07-02
Model NumberZM-920PA
Catalog NumberZM-920PA
Lot NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Age179 MO
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerNIHON KOHDEN CORPORATION
Manufacturer Address1-31-4 NISHIOCHIA, SHINJUKU-KU ATTN: SHAMA MOOMAN TOKYO, 161-8560 JA 161-8560


Patients

Patient NumberTreatmentOutcomeDate
10 2019-07-02

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