Publicidad
Idiomas disponibles
Idiomas disponibles
10.3 Conformité CE
Ce produit répond aux exigences de la directive européenne 93/42/CEE relative aux dispositifs
médicaux. Le produit a été classé dans la classe I sur la base des critères de classification
d'après l'annexe IX de cette directive. La déclaration de conformité a donc été établie par le fabri
cant sous sa propre responsabilité, conformément à l'annexe VII de la directive.
Le soussigné, Ottobock Healthcare Products GmbH, déclare que le présent produit est conforme
à la directive 2014/53/UE. Le texte complet de la déclaration de conformité CE est disponible à
l'adresse Internet suivante : www.ottobock.com/conformity
Le produit est conforme aux exigences applicables de la directive 2011/65/UE relative à la limita
tion de l'utilisation de certaines substances dangereuses dans les équipements électriques et
électroniques (« RoHS »).
10.4 Informations légales locales
Les informations légales applicables exclusivement dans des pays individuels figurent dans la
langue officielle du pays d'utilisation en question dans ce chapitre.
This device complies with part 15 of the FCC Rules. Operation is subject to the following two
conditions:
1) This device may not cause harmful interference, and
2) This device must accept any interference received, including interference that may cause unde
sired operation.
This equipment has been tested and found to comply with the limits for a Class B digital device,
pursuant to part 15 of the FCC Rules. These limits are designed to provide reasonable protection
against harmful interference in a residential installation. This equipment generates uses and can
radiate radio frequency energy and, if not installed and used in accordance with the instructions,
may cause harmful interference to radio communications. However, there is no guarantee that in
terference will not occur in a particular installation. If this equipment does cause harmful interfe
rence to radio or television reception, which can be determined by turning the equipment off and
on, the user is encouraged to try to correct the interference by one or more of the following mea
sures:
—Reorient or relocate the receiving antenna.
—Increase the separation between the equipment and receiver.
—Connect the equipment into an outlet on a circuit different from that to which the receiver is
connected.
—Consult the dealer or an experienced radio/ TV technician for help.
Any changes or modifications not expressly approved by the party responsible for compliance
could void the user's authority to operate the equipment.
Caution: Exposure to Radio Frequency Radiation.
This device must not be co-located or operating in conjunction with any other antenna or transmit
ter.
Responsible party:
Otto Bock Health Care, LP
3820 West Great Lakes Drive
Salt Lake City, Utah 84120-7205 USA
Phone + 1-801-956-2400
Fax + 1-801-956-2401
This device complies with RSS 210 of Industry Canada.
Operation is subject to the following two conditions:
85
Publicidad
