B BRAUN SPINAL KIT

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-07-31 for B BRAUN SPINAL KIT manufactured by B. Braun Medical Inc..

MAUDE Entry Details

Report NumberMW5088655
MDR Report Key8855669
Date Received2019-07-31
Date of Report2019-07-26
Date of Event2019-07-08
Date Added to Maude2019-08-02
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 Sequence Number: 1

Brand NameB BRAUN SPINAL KIT
Generic NameSPINAL ANESTHESIA KIT
Product CodeOFU
Date Received2019-07-31
Lot Number0061663567
Device AvailabilityY
Device Eval'ed by MfgrI
Device Sequence No1
Device Event Key0
ManufacturerB. BRAUN MEDICAL INC.

Device Sequence Number: 2

Brand NameB BRAUN SPINAL KIT
Generic NameSPINAL ANESTHESIA KIT
Product CodeOFU
Date Received2019-07-31
Lot Number0061663567
Device AvailabilityY
Device Eval'ed by MfgrI
Device Sequence No2
Device Event Key0
ManufacturerB. BRAUN MEDICAL INC.

Device Sequence Number: 3

Brand NameB BRAUN SPINAL KIT
Generic NameSPINAL ANESTHESIA KIT
Product CodeOFU
Date Received2019-07-31
Lot Number0061663567
Device AvailabilityY
Device Eval'ed by MfgrI
Device Sequence No3
Device Event Key0
ManufacturerB. BRAUN MEDICAL INC.

Device Sequence Number: 4

Brand NameB BRAUN SPINAL KIT
Generic NameSPINAL ANESTHESIA KIT
Product CodeOFU
Date Received2019-07-31
Lot Number0061663567
Device AvailabilityY
Device Eval'ed by MfgrI
Device Sequence No4
Device Event Key0
ManufacturerB. BRAUN MEDICAL INC.


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-07-31

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