IMMULITE 2000 HUMAN CHORIONIC GONADOTROPIN (HCG) ASSAY 10381206

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,u report with the FDA on 2020-03-02 for IMMULITE 2000 HUMAN CHORIONIC GONADOTROPIN (HCG) ASSAY 10381206 manufactured by Siemens Healthcare Diagnostics Products, Limited.

MAUDE Entry Details

Report Number2432235-2020-00221
MDR Report Key9775860
Report SourceFOREIGN,HEALTH PROFESSIONAL,U
Date Received2020-03-02
Date of Report2020-03-02
Date of Event2019-12-21
Date Mfgr Received2020-02-06
Date Added to Maude2020-03-02
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. MIR KHAN
Manufacturer Street511 BENEDICT AVENUE
Manufacturer CityTARRYTOWN, NY
Manufacturer CountryUS
Manufacturer Phone5243074
Manufacturer G1SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, LIMITED
Manufacturer StreetGLYN RHONWY UK REGISTRATION #: 3002806944
Manufacturer CityLLANBERIS, LL554EL
Manufacturer CountryUK
Manufacturer Postal CodeLL55 4EL
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameIMMULITE 2000 HUMAN CHORIONIC GONADOTROPIN (HCG) ASSAY
Generic NameHUMAN CHORIONIC GONADOTROPIN (HCG) ASSAY
Product CodeDHA
Date Received2020-03-02
Model NumberIMMULITE 2000 HUMAN CHORIONIC GONADOTROPIN
Catalog Number10381206
Lot Number402
Device Expiration Date2020-02-29
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerSIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, LIMITED
Manufacturer AddressGLYN RHONWY LLANBERIS, LL554EL UK LL55 4EL


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-02

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