OPTIGUN RATCHET 4195

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2018-07-04 for OPTIGUN RATCHET 4195 manufactured by Biomet France S.a.r.l..

Event Text Entries

[113187063] (b)(4). The investigation is in process. Once the investigation has been completed, a follow-up mdr will be submitted. Lot number not communicated.
Patient Sequence No: 1, Text Type: N, H10


[113187064] It has been reported that it was not possible to press the cement out when cylinder was put in the gun.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3006946279-2018-00241
MDR Report Key7662237
Report SourceUSER FACILITY
Date Received2018-07-04
Date of Report2018-07-04
Date Mfgr Received2018-06-11
Date Added to Maude2018-07-04
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. H BATAILLE
Manufacturer StreetPLATEAU DE LAUTAGNE BP75
Manufacturer CityVALENCE 26903
Manufacturer CountryFR
Manufacturer Postal26903
Manufacturer Phone0334757591
Manufacturer G1BIOMET FRANCE S.A.R.L.
Manufacturer StreetPLATEAU DE LAUTAGNE BP75
Manufacturer CityVALENCE CEDEX 26903
Manufacturer CountryFR
Manufacturer Postal Code26903
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameOPTIGUN RATCHET
Generic NameDISPENSER, CEMENT
Product CodeKIH
Date Received2018-07-04
Catalog Number4195
Lot NumberNOT COMMUNICATED
ID Number(01) 07350023771603
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBIOMET FRANCE S.A.R.L.
Manufacturer AddressPLATEAU DE LAUTAGNE BP75 VALENCE CEDEX 26903 FR 26903


Patients

Patient NumberTreatmentOutcomeDate
10 2018-07-04

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