Contraindications - Bego IDC Gebrauchsanweisung

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Indications for use:
The IDC (implant adjustment instrument) is used exclusively in patients who have been
implanted with a BEGO Semados
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Platform Switch Design such as the RS/RSX implant. The diameter of the instrument
chosen depends on the implant diameter. Remove any contamination at the implant
site before attaching the instrument. The IDC is inserted into the implant up to the stop,
at which point the hex of the IDC engages with the internal hex of the implant. BEGO
Semados instruments are packaged non-sterile and must be processed before using
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them for the first time and immediately after each application using a process that
has been adequately validated specifically for the device and the product so as not
to endanger the patient as a result of the application. Please follow the 'Processing
Instructions for BEGO Semados Trays' for this purpose. Unprotected contact with the
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BEGO Semados instruments by the user both before and after sterilisation must be
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avoided (use protective gloves). The IDC has a socket for the 'Implant Insertion Tool'
and can be used, after selecting the corresponding 'Implant Insertion Tool', with either
the handpiece/contra-angle or the ratchet/torque wrench. The position of the internal
hex of the implant can also be read on the 'Implant Insertion Tool' when using the IDC.
Damaged instruments must be replaced immediately (please follow the 'Processing
Instructions for BEGO Semados Trays' to do this). In case of doubt, instruments should
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always be replaced earlier. Improper use of the BEGO Semados
to premature wear and tear of the instruments and may pose a risk to the user and/
or the patient.
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S/RI implant or a BEGO Semados implant with the
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instruments can lead
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Contraindications:

Known incompatibilities or allergies to any of the material constituents.
Warnings:
Do not use the IDC (implant adjustment instrument) under any circumstances to
fully insert an implant but use it only to make the final correction of the position after
implantation is complete. Pay close attention to the seating of the IDC on the implant,
ensuring there is no gap. Do not exert a bending moment on the IDC. The implants may
only actually be inserted in the BEGO implant system using the insertion post already
mounted on the implant when delivered. If very high tightening moments (> 50 Ncm)
develop, the implant must be removed, because of risk of damage to the implant or
the ratchet, and set aside while kept sterile. The implant bed must be prepared again
as necessary to adjust the depth, drill hole diameter, bone thread or countersink for
the head. The
surface connecting to the implant must not be blasted or processed. The fit is predeter-
mined according to industrial specifications.
Precautions:
It is recommended that the patient is protected from the risk of aspiration or swallowing
of the parts. Ensure that only handpieces and contra-angles are used that are techni-
cally and hygienically faultless and have been maintained and cleaned.
Adverse reactions / interactions:
In rare isolated cases, allergies to constituents of the materials (see Product Informa-
tion) or electrochemically-induced dysaesthesia may occur. In case of occlusal or proxi-
mal contact between different materials, dysaesthesia may occur in rare isolated cases.
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