JAW INS.MICRO-DISSECTOR SCISS 5MM 310MM PO602R

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2017-12-21 for JAW INS.MICRO-DISSECTOR SCISS 5MM 310MM PO602R manufactured by Aesculap Ag.

Event Text Entries

[95619545] (b)(4). Manufacturing site evaluation: evaluation on-going. Device not returned
Patient Sequence No: 1, Text Type: N, H10


[95619546] (b)(6). During procedure for gynecology, jaw was broken. When cutting a suture, blades crossed. After that, blades opened beyond normal range using for procedure. By x-ray, any metal fragments were not found in the abdominal cavity. No injury for the patient has been currently reported. Components in use listed as concomitant devices are: po602r / jaw ins. Micro-dissector sciss 5mm 310mm, pm973r / nsulated outer tube 5/5mm 310mm, po958r / monopolar handle without ratchet.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9610612-2017-00630
MDR Report Key7138921
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2017-12-21
Date of Report2018-01-19
Date of Event2017-12-18
Date Facility Aware2017-12-21
Date Mfgr Received2017-12-19
Date Added to Maude2017-12-21
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 FDA3
Event Location3
Manufacturer ContactMS. NICOLE BROYLES
Manufacturer Street615 LAMBERT POINTE DRIVE
Manufacturer CityHAZELWOOD MO 63042
Manufacturer CountryUS
Manufacturer Postal63042
Manufacturer Phone3145515988
Manufacturer G1AESCULAP AG
Manufacturer StreetPO BOX 40
Manufacturer CityTUTTLINGEN, 78501
Manufacturer CountryGM
Manufacturer Postal Code78501
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameJAW INS.MICRO-DISSECTOR SCISS 5MM 310MM
Generic NameENDOSCOPY
Product CodeKNF
Date Received2017-12-21
Model NumberPO602R
Catalog NumberPO602R
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerAESCULAP AG
Manufacturer AddressPO BOX 40 TUTTLINGEN, 78501 GM 78501


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2017-12-21

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