CUSA EXCEL 23KHZ LAPAROSCOPIC TIP ELT C4604ELT

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2013-10-31 for CUSA EXCEL 23KHZ LAPAROSCOPIC TIP ELT C4604ELT manufactured by Integra Burlington, Ma, Inc..

Event Text Entries

[15264998] It was reported that a c4604elt separated during a first run test. There was no pt involvement and no injury.
Patient Sequence No: 1, Text Type: D, B5


[15785498] To date, the device involved in the reported incident has not been received for evaluation. An investigation has been initiated based upon the reported information.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number3006697299-2013-00073
MDR Report Key3558384
Report Source05
Date Received2013-10-31
Date of Report2013-10-31
Date Mfgr Received2013-10-01
Date Added to Maude2014-01-31
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactLINDA SERENTINO
Manufacturer Street315 ENTERPRISE DRIVE
Manufacturer Phone6099365560
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCUSA EXCEL 23KHZ LAPAROSCOPIC TIP ELT
Generic NameULTRASONIC SURGICAL PRODUCTS
Product CodeLBK
Date Received2013-10-31
Catalog NumberC4604ELT
Lot NumberTL-283420
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerINTEGRA BURLINGTON, MA, INC.
Manufacturer AddressBURLINGTON MA 01803 US 01803


Patients

Patient NumberTreatmentOutcomeDate
10 2013-10-31

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