12.5F X 15CM HEMO-CATH MC101241

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 2020-02-19 for 12.5F X 15CM HEMO-CATH MC101241 manufactured by Medical Components, Inc..

MAUDE Entry Details

Report Number2518902-2020-00008
MDR Report Key9727528
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2020-02-19
Date of Report2020-02-19
Date Mfgr Received2020-01-28
Device Manufacturer Date2019-10-10
Date Added to Maude2020-02-19
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 Street1499 DELP DRIVE
Manufacturer CityHARLEYSVILLE PA 19438
Manufacturer CountryUS
Manufacturer Postal19438
Manufacturer Phone2152564201
Manufacturer G1MEDICAL COMPONENTS, INC.
Manufacturer Street1499 DELP DRIVE
Manufacturer CityHARLEYSVILLE PA 19438
Manufacturer CountryUS
Manufacturer Postal Code19438
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand Name12.5F X 15CM HEMO-CATH
Generic NameHEMO-CATH
Product CodeMSD
Date Received2020-02-19
Model NumberMC101241
Catalog NumberMC101241
Lot NumberMNRV060
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerMEDICAL COMPONENTS, INC.
Manufacturer Address1499 DELP DRIVE HARLEYSVILLE PA 19438 US 19438


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-19

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.