VM T-COAT MICRO HDL KERRISON RONGEUR THIN 8IN 1 MM NL4252-81T / 2110814BT

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor report with the FDA on 2018-06-20 for VM T-COAT MICRO HDL KERRISON RONGEUR THIN 8IN 1 MM NL4252-81T / 2110814BT manufactured by S.u.a. Martin Gmbh &co.kg.

Event Text Entries

[111987924] A deep dent in the cutting edge indicates that the instrument was used to cut hard material, such as wire. Evaluation is in progress. Should additional information become available, a follow-up report will be submitted.
Patient Sequence No: 1, Text Type: N, H10


[111987925] The device broke while being used in the patient's neck during an acdf procedure. The broken piece of the device jaw fell into the neck and was retrieved with the suction and a forceps. There was no harm to the patient nor the doctor. The procedure was completed as planned.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number8010386-2018-00006
MDR Report Key7619783
Report SourceDISTRIBUTOR
Date Received2018-06-20
Date of Report2018-06-29
Date of Event2018-04-10
Date Mfgr Received2018-06-21
Device Manufacturer Date2017-02-24
Date Added to Maude2018-06-20
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 ContactMR. MARKUS PAULI
Manufacturer StreetUHLANDSTRASSE 17
Manufacturer CityRIETHEIM-WEILHEIM, 78604
Manufacturer CountryGM
Manufacturer Postal78604
Manufacturer G1S.U.A. MARTIN GMBH &CO.KG
Manufacturer StreetUHLANDSTRASSE 17
Manufacturer CityRIETHEIM-WEILHEIM, 78604
Manufacturer CountryGM
Manufacturer Postal Code78604
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameVM T-COAT MICRO HDL KERRISON RONGEUR THIN 8IN 1 MM
Generic NameMANUAL RONGEUR
Product CodeHAE
Date Received2018-06-20
Catalog NumberNL4252-81T / 2110814BT
Lot NumberC17XME
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerS.U.A. MARTIN GMBH &CO.KG
Manufacturer AddressUHLANDSTRASSE 17 RIETHEIM-WEILHEIM, 78604 GM 78604


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2018-06-20

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.