3M? CUROS? DISINFECTING CAP FOR NEEDLELESS CONNECTORS CFF10-250

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-09-26 for 3M? CUROS? DISINFECTING CAP FOR NEEDLELESS CONNECTORS CFF10-250 manufactured by 3m Health Care.

MAUDE Entry Details

Report Number2110898-2019-00114
MDR Report Key9122572
Date Received2019-09-26
Date of Report2019-09-26
Date of Event2019-08-24
Date Mfgr Received2019-09-13
Date Added to Maude2019-09-26
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA0
Report to FDA3
Event Location3
Manufacturer ContactDIANNE GIBBS
Manufacturer Street2510 CONWAY AVE 3M CENTER BUILDING 275-5W-06
Manufacturer CityST. PAUL MN 55144
Manufacturer CountryUS
Manufacturer Postal55144
Manufacturer Phone6517379117
Manufacturer G13M COMPANY 3M COLUMBIA
Manufacturer Street5400 PARIS ROAD
Manufacturer CityCOLUMBIA MO 65202
Manufacturer CountryUS
Manufacturer Postal Code65202
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand Name3M? CUROS? DISINFECTING CAP FOR NEEDLELESS CONNECTORS
Generic NameCUROS DISINFECTING CAP FOR NEEDLELESS CONNECTORS
Product CodeQBP
Date Received2019-09-26
Catalog NumberCFF10-250
Lot NumberUNK
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
Manufacturer3M HEALTH CARE
Manufacturer Address2510 CONWAY AVE ST. PAUL MN 55144 US 55144


Patients

Patient NumberTreatmentOutcomeDate
10 2019-09-26

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