Philips NFCBV1 User Manual

Philips Medizin Systeme Böblingen GmbH
Hewlett-Packard-Strasse 2, 71034 Böblingen, Germany, Tel +49(0)7031 463-0, Fax +49(0)7031 463-2202 Geschäftsführer: Dr. Dieter Haase (Sprecher), Dr. Peter Ziese, Matthijs de Groot Registergericht Stuttgart Reg.-Nr. HRB 245187, Sitz der Gesellschaft: Böblingen, www.philips.com/healthcare
NFCBV1-A NFC Module User Manual
Model: NFCBV1-A FCC-ID: PQC-NFCBV1 IC: 3549C-NFCBV1
For OEM integration only – device cannot be sold to general public. Therefore, we will not supply a user manual.
We will ask OEM to include the following notices required by FCC/IC on the product and in the user manual.
Manual Requirements according 15.105
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 interference will not occur in a particular installation. If this equipment does cause harmful interference 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 measures:
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.
Manual Requirements according 15.19 / RSS-GEN
This device complies with Part 15 of the FCC Rules and with Industry Canada licence-exempt RSS standard(s).
Operation is subject to the following two conditions:
this device may not cause harmful interference, and  this device must accept any interference received, including interference that may cause
undesired operation.
Philips Medizin Systeme Böblingen GmbH
Hewlett-Packard-Strasse 2, 71034 Böblingen, Germany, Tel +49(0)7031 463-0, Fax +49(0)7031 463-2202 Geschäftsführer: Dr. Dieter Haase (Sprecher), Dr. Peter Ziese, Matthijs de Groot Registergericht Stuttgart Reg.-Nr. HRB 245187, Sitz der Gesellschaft: Böblingen, www.philips.com/healthcare
Le présent appareil est conforme aux CNR d'Industrie Canada applicables aux appareils radio exempts de licence. L'exploitation est autorisée aux deux conditions suivantes:
l'appareil ne doit pas produire de brouillage, et  l'appareil doit accepter tout brouillage radioélectrique subi, même si le brouillage est susceptible
d'en compromettre le fonctionnement.
Manual Requirements according 15.21
Changes or modifications made to this equipment not expressly approved by (manufacturer name) may void the FCC authorization to operate this equipment.
RF Exposure Information according 2.1091 / 2.1093 / KDB 447498 / RSS-102
This equipment complies with FCC and IC radiation exposure limits set forth for an uncontrolled environment. This equipment should be installed and operated with minimum distance of 20 cm between the radiator and your body.
This transmitter must not be co-located or operating in conjunction with any other antenna or transmitter.
Cet équipement est conforme aux limites d'exposition aux rayonnements IC établies pour un environnement non contrôlé. Cet équipement doit être installé et utilisé avec un minimum de 20 cm de distance entre la source de rayonnement et votre corps.
Ce transmetteur ne doit pas etre place au meme endroit ou utilise simultanement avec un autre transmetteur ou antenne.
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