CADIAX compact
18
Only use accessories which are explicitly approved for CADIAX devices. Using other ac-
cessories, especially cables which are longer than the cable lengths prescribed below,
can lead to increased emission of interferences, or to reduced interference immunity of
the CADIAX device, which may lead to faulty operation.
The following accessories to the CADIAX system affect the system's electromagnetic compatibility and
may be replaced by the user. Components not listed here may only be replaced by the manufacturer.
Accessory
Maximum cable length
Foot switch
3.0 m
USB cable (USB 2.0, type A plug to type B plug, shielded)
3.0 m
CADIAX "compact" sensors
1.5 m
CADIAX "diagnostic" stylus (only applicable to CADIAX 4 devices)
1.5 m
CADIAX "diagnostic" flag (only applicable to CADIAX 4 devices)
1.5 m
Portable and mobile HF-communication appliances, e.g., mobile telephones, cordless
telephones, computers, and laptops with activated WiFi, etc., can have detrimental ef-
fects on medical electrical devices. Do not operate the CADIAX device in the proximity of
these potential sources of interference, and make sure to adhere to a safe distance of at
least 30 cm. Non-compliance can lead to reduced performance of the device.
1.2.2.7
Connecting other devices
Devices connected to analog or digital interfaces must be certified to satisfy the applic-
able standard EN specifications (e.g., EN 60950 for data-processing devices, or EN
60601 for medical electrical devices). In addition, all configurations must satisfy system
standard EN 60601-1. Whoever connects supplementary devices to the signal input or
outlet units is the system configurator and therefore responsible for ensuring that system
standard EN 60601-1 is adhered to.
1.2.3
Contraindications - Limitations to application
When operating the CADIAX system, the following conditions can hinder or limit its ap-
plication:
·
Cognitive abilities:
Patients who are not able to follow or carry out the attending dent-
ist's instructions correctly (e.g., where to move the lower jaw, etc.), for physical or psy-
chological reasons.
·
General clinical symptoms:
Patients with illnesses that do not allow for the attach-
ment of a face bow for registration purposes. Illnesses may be physical or psycholo-
gical in nature (e.g., spastic, epilepsy, claustrophobia, injury or disease of the skull or
soft-tissue structures of the skull, ears, etc.).
·
Dental clinical symptoms:
Patients with odontopathy or periodontal disease, which
excludes the mounting of a clutch (parodontosis, loose teeth, damage to the tooth sub-
stance, changes in the mucous membranes in the mouth or pharynx, etc.).
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