DYNAMIC INLET, PLC (BULK READY), POWER EXPRESS B90918

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 2019-08-29 for DYNAMIC INLET, PLC (BULK READY), POWER EXPRESS B90918 manufactured by Beckman Coulter.

MAUDE Entry Details

Report Number2050012-2019-01101
MDR Report Key8945310
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2019-08-29
Date of Report2019-08-28
Date of Event2018-01-19
Date Facility Aware2018-01-19
Date Mfgr Received2018-01-19
Device Manufacturer Date2017-03-01
Date Added to Maude2019-08-29
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. DAVID DAVIS
Manufacturer Street250 S. KRAEMER BLVD.
Manufacturer CityBREA CA 928218000
Manufacturer CountryUS
Manufacturer Postal928218000
Manufacturer Phone7149613796
Manufacturer G1BECKMAN COULTER
Manufacturer Street250 S. KRAEMER BLVD.
Manufacturer CityBREA CA 928218000
Manufacturer CountryUS
Manufacturer Postal Code928218000
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameDYNAMIC INLET, PLC (BULK READY), POWER EXPRESS
Generic NameRADIOASSAY, VITAMIN B12
Product CodeCDD
Date Received2019-08-29
Model NumberDYNAMIC INLET, PLC (BULK READY), POWER EXPRESS
Catalog NumberB90918
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerBECKMAN COULTER
Manufacturer Address250 S. KRAEMER BLVD. BREA CA 928218000 US 928218000


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-08-29

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