PIEZOSURGERY MT1-10 03600001

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-02-20 for PIEZOSURGERY MT1-10 03600001 manufactured by Mectron S.p.a..

Event Text Entries

[139069977] The manufacturer mectron s. P. A. Received the insert involved in the event. An investigation was carry out by the manufacturer: the insert returned mt1-10, lot. Number 18002205 was analysed by an external laboratory. The result of this analysis didn't reveal any critical problem on the structure of the insert. Moreover the design, production, in -process an final controls documents, related to the insert mt1-10, lot. Number 18002205, didn't show any anomaly.
Patient Sequence No: 1, Text Type: N, H10


[139069978] During the use in the maxillofacial surgery the insert mt1-10, lot. N. 18002205, broke. No adverse event occurred to the patient. More information about this insert: eto sterilization batch n. (b)(4); expiration date : july/30/2023.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3003933619-2018-00008
MDR Report Key8353086
Date Received2019-02-20
Date of Report2018-01-09
Date of Event2018-10-12
Date Mfgr Received2018-10-12
Device Manufacturer Date2018-07-30
Date Added to Maude2019-02-20
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 ContactMS. GIOVANNA ROMEO
Manufacturer StreetVIA LORETO 15/A /
Manufacturer CityCARASCO, GENOA 16042
Manufacturer CountryIT
Manufacturer Postal16042
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NamePIEZOSURGERY
Generic NameMT1 -10, IINSERT FOR GENERAL BONE SURGERY
Product CodeJDX
Date Received2019-02-20
Returned To Mfg2018-11-12
Model NumberMT1-10
Catalog Number03600001
Lot Number18002205
Device Expiration Date2018-07-30
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerMECTRON S.P.A.
Manufacturer AddressVIA LORETO 15/A / CARASCO, GENOA 16042 IT 16042


Patients

Patient NumberTreatmentOutcomeDate
10 2019-02-20

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