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Air Techniques, Inc.
Classic, Ortho & Intraoral
Markings
.
The following terms or symbols are used on the equipment or in this manual to denote information of
special importance:
Cautions
(Continued)-
Completely clean and erase PSPs before taking an X-ray exposure.
See the PLATE PREPARATION section of this manual .
Minimize exposing an X-ray exposed PSP to light.
Transfer the PSP into the inlet slot quickly to
minimize exposure to light .
Use care in handling PSPs - Avoid fingerprints and scratching.
Refer to the instructions provided with the PSP package for further information on handling .
Use of other manufacturer’s imaging plates.
Do not put PSPs designed for drum-type or other
scanners in the ScanX . The hooks and/or frames on the ends or around these PSPs, or PSPs of different
thickness (especially thicker ones) will damage the ScanX .
Contraindications
. None known .
GENERAL SAFETY
DANGER
AVOID DIRECT
EXPOSURE TO BEAM
LASER RADIATION WHEN OPEN
CAUTION
CLASS 1 LASER PRODUCT
CLASS 3B LASER
RADIATION WHEN OPEN
AVOID EXPOSURE TO BEAM
CLASS IIIb LASER PRODUCT
COVER REMOVED MAKES
THIS DEVICE A
ScanX is a Class I Laser Product [Class 1 Laser Product (IEC)]
This warning label identifies ScanX as such a product and describes
the potential danger to humans in the event the product is opened during
service. There is no laser radiation from this product when operated and
maintained as instructed.
The Laser Product Accession Number is 0212282-00
Alerts users to important Operating and
Maintenance instructions. Read carefully
to avoid any problems.
Indicates date
of manufacture
Identifies the
name of the
manufacturer.
Warns users that uninsulated voltage
within the unit may be of sufficient
magnitude to cause electric shock.
Indicates that ScanX complies with the
Medical Device Directive 93/42/EEC.
Indicates that the unit conforms with
WEEE Directive 2002/96/EC and must be
disposed of only at the appropriate facilities
for recovery and recycling.
Manufacturer:
Air Techniques, Inc.
1295 Walt Whitman Road
Melville, New York 11747 USA
Medical Device Safety Service
Schiffgraben 41
30175 Hannover, Germany
EC REP
Indicates item used only
once. Discard after use.
2
Indicates the
ScanX is a UL
Listed product .
LABORATORY
EQUIPMENT
60CB
E234737