SUCTION TUBING 3604240 N512

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-07-12 for SUCTION TUBING 3604240 N512 manufactured by Cardinal Health Malta 212 Ltd.

MAUDE Entry Details

Report NumberMW5088116
MDR Report Key8790767
Date Received2019-07-12
Date of Report2019-04-22
Date of Event2019-04-18
Date Added to Maude2019-07-15
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationRISK MANAGER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameSUCTION TUBING
Generic NameTUBING, NONINVASIVE
Product CodeGAZ
Date Received2019-07-12
Model Number3604240
Catalog NumberN512
Lot NumberJ18111235S
OperatorHEALTH PROFESSIONAL
Device Availability*
Device Eval'ed by MfgrI
Device Sequence No1
Device Event Key0
ManufacturerCARDINAL HEALTH MALTA 212 LTD


Patients

Patient NumberTreatmentOutcomeDate
10 2019-07-12

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