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  9. Ivy Biomedical Systems 580076 Owner's manual

Ivy Biomedical Systems 580076 Owner's manual

__________________________________________________________________________________________________
Ivy Biomedical Systems, Inc. | 11 Business Park Drive | Branford, CT 06405
P 203.481.4183 | F 203.481.8734 | www.ivybiomedical.com
580076
Regulatory Information
1CURRENT REGULATORY CERTIFICATIONS
The 580076 holds current certifications in the following countries:
Country/Region Regulatory ID
USA (FCC) 15.247 2A3IX-WGS100
Canada (ISED) RSS-247 Issue 2 27829-WGS100
2CERTIFIED ANTENNAS
Part Number Mfg. Type Connector Gain (dBi)
001-0001 Laird Connectivity Dipole U.FL to RPSMA cable 2 dBi (2400 MHz-2480 MHz)
001-0014 Laird Connectivity PIFA IPEX U.FL 2 dBi (2400 MHz-2480 MHz)
001-0015 Laird Connectivity FlexNotch IPEX U.FL 2 dBi (2400 MHz-2480 MHz)
001-0030 Laird Connectivity PIFA IPEX U.FL 2 dBi (2400 MHz-2480 MHz)
N/A Laird Connectivity PCB printed N/A 0 dBi
Note: The OEM is free to choose another vendor’s antenna of like type and equal or lesser gain as an antenna appearing
in the table and still maintain compliance. Reference FCC Part 15.204(c)(4) for further information on this topic.
To reduce potential radio interference to other users, the antenna type and gain should be chosen so that the equivalent
isotropic radiated power (EIRP) is not more than that permitted for successful communication.
3FCC REGULATORY
3.1 Federal Communication Commission Interference Statement
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 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.
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 undesired operation.
This portable transmitter with its antenna complies with FCC/IC RF exposure limits for general population/
uncontrolled exposure.
__________________________________________________________________________________________________
Ivy Biomedical Systems, Inc. | 11 Business Park Drive | Branford, CT 06405
P 203.481.4183 | F 203.481.8734 | www.ivybiomedical.com
FCC Caution: Any changes or modifications not expressly approved by the party responsible for compliance could void the
user's authority to operate this equipment.
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 undesired operation.
IMPORTANT NOTE:
FCC Radiation Exposure Statement:
The product complies with the US portable RF exposure limit set forth for an uncontrolled environment and are safe for
intended operation as described in this manual. The further RF exposure reduction can be achieved if the product can be kept
as far as possible from the user body or set the device to lower output power if such function is available.
This transmitter must not be co-located or operating in conjunction with any other antenna or transmitter.
This device is intended only for OEM integrators under the following condition:
1. The transmitter module may not be co-located with any other transmitter or antenna,
Since this module and its associated set of approved antennas have been certified as a Modular Radio, this allows the end
user to integrate this module into an end-product without the requirement of re-certifying the radio module. The module-
integrator is responsible for the unintentional conducted and radiated emissions and must verify that the integrated product is
compliant with the rules associated with unintentional radiators. FCC also expects integrators to do spot checking of
transmitter tests as necessary based upon KDB 996369 D04. The module integrator is also required to maintain an
engineering record of the verification testing and declare on the product through proper labeling and marking that the device is
compliant with these particular rules.
IMPORTANT NOTE
If this condition cannot be met (for example, certain laptop configurations or co-location with another transmitter), then the
FCC authorization is no longer considered valid and the FCC ID cannot be used on the final product. In these circumstances,
the OEM integrator is responsible for re-evaluating the end product (including the transmitter) and obtaining a separate FCC
authorization.
End Product Labeling
The final end product must be labeled in a visible area with the following: “Contains FCC ID:2A3IX-WGS100”.
Manual Information to the End User
The OEM integrator has to be aware not to provide information to the end user regarding how to install or remove this RF
module in the user’s manual of the end product which integrates this module.
The end user manual shall include all required regulatory information/warning as show in this manual.
__________________________________________________________________________________________________
Ivy Biomedical Systems, Inc. | 11 Business Park Drive | Branford, CT 06405
P 203.481.4183 | F 203.481.8734 | www.ivybiomedical.com
4ISED (CANADA)REGULATORY
4.1 ISED Canada Statement
This device complies with Industry Canada’s license-exempt RSSs. Operation is subject to the following two conditions:
1. This device may not cause interference; and
2. This device must accept any interference, including interference that may cause undesired operation of the device.
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:
1. l’appareil ne doit pas produire de brouillage;
2. l’utilisateur de l’appareil doit accepter tout brouillage radioélectrique subi, même si le brouillage est susceptible d’en
compromettre le fonctionnement.
Radiation Exposure Statement:
The product complies with the Canada portable RF exposure limit set forth for an uncontrolled environment and are safe for
intended operation as described in this manual. The minimum separation distance for portable use is limited to 15mm
assuming use of antenna with 2dBi of gain. The further RF exposure reduction can be achieved if the product can be kept as
far as possible from the user body or set the device to lower output power if such function is available.
Déclaration d'exposition aux radiations:
Le produit est conforme aux limites d'exposition pour les appareils portables RF pour les Etats-Unis et le Canada établies pour
un environnement non contrôlé. La distance de séparation minimale pour l'utilisation portative est limitée à 15mm en
supposant l'utilisation de l'antenne avec 2dBi de gain. Le produit est sûr pour un fonctionnement tel que décrit dans ce
manuel. La réduction aux expositions RF peut être augmentée si l'appareil peut être conservé aussi loin que possible du corps
de l'utilisateur ou que le dispositif est réglé sur la puissance de sortie la plus faible si une telle fonction est disponible.
This device is intended only for OEM integrators under the following conditions:
1. The transmitter module may not be co-located with any other transmitter or antenna.
If the condition above is met, further transmitter testing is not required. However, the OEM integrator is still responsible for
testing their end-product for any additional compliance requirements required with this module installed.
Cet appareil est conçu uniquement pour les intégrateurs OEM dans les conditions suivantes:
1. Le module émetteur peut ne pas être coïmplanté avec un autre émetteur ou antenne.
Tant que les 1 condition ci-dessus sont remplies, des essais supplémentaires sur l'émetteur ne seront pas nécessaires.
Toutefois, l'intégrateur OEM est toujours responsable des essais sur son produit final pour toutes exigences de conformité
supplémentaires requis pour ce module installé.
IMPORTANT NOTE:
In the event that these conditions cannot be met (for example certain laptop configurations or co-location with another
transmitter), then the Canada authorization is no longer considered valid and the IC ID cannot be used on the final product. In
these circumstances, the OEM integrator will be responsible for re-evaluating the end product (including the transmitter) and
obtaining a separate Canada authorization.
NOTE IMPORTANTE:
Dans le cas où ces conditions ne peuvent être satisfaites (par exemple pour certaines configurations d'ordinateur portable ou
de certaines co-localisation avec un autre émetteur), l'autorisation du Canada n'est plus considéré comme valide et l'ID IC ne
peut pas être utilisé sur le produit final. Dans ces circonstances, l'intégrateur OEM sera chargé de réévaluer le produit final (y
compris l'émetteur) et l'obtention d'une autorisation distincte au Canada.
End Product Labeling
The final end product must be labeled in a visible area with the following: “Contains IC: 27829-WGS100”.
Plaque signalétique du produit final
Le produit final doit être étiqueté dans un endroit visible avec l'inscription suivante: "Contient des IC:27829-WGS100”.
__________________________________________________________________________________________________
Ivy Biomedical Systems, Inc. | 11 Business Park Drive | Branford, CT 06405
P 203.481.4183 | F 203.481.8734 | www.ivybiomedical.com
Manual Information to the End User
The OEM integrator has to be aware not to provide information to the end user regarding how to install or remove this RF
module in the user’s manual of the end product which integrates this module.
The end user manual shall include all required regulatory information/warning as show in this manual.
Manuel d'information à l'utilisateur final
L'intégrateur OEM doit être conscient de ne pas fournir des informations à l'utilisateur final quant à la façon d'installer ou de
supprimer ce module RF dans le manuel de l'utilisateur du produit final qui intègre ce module.
Le manuel de l'utilisateur final doit inclure toutes les informations réglementaires requises et avertissements comme indiqué
dans ce manuel.
This radio transmitter IC: 27829-WGS100 has been approved by Innovation, Science and Economic Development Canada to
operate with the antenna types listed below, with the maximum permissible gain indicated. Antenna types not included in this
list that have a gain greater than the maximum gain indicated for any type listed are strictly prohibited for use with this device.
Cet émetteur radio IC : 27829-WGS100 a été approuvé par Innovation, Sciences et Développement économique Canada pour
fonctionner avec les types d'antennes répertoriés ci-dessous, avec le gain maximal autorisé indiqué. Les types d'antenne non
inclus dans cette liste qui ont un gain supérieur au gain maximum indiqué pour tout type répertorié sont strictement interdits
pour une utilisation avec cet appareil.
Part Number Mfg. Type Connector Gain (dBi)
001-0001 Laird Connectivity Dipole U.FL to RPSMA cable 2 dBi (2400 MHz-2480 MHz)
001-0014 Laird Connectivity PIFA IPEX U.FL 2 dBi (2400 MHz-2480 MHz)
001-0015 Laird Connectivity FlexNotch IPEX U.FL 2 dBi (2400 MHz-2480 MHz)
001-0030 Laird Connectivity PIFA IPEX U.FL 2 dBi (2400 MHz-2480 MHz)
N/A Laird Connectivity PCB printed N/A 0 dBi
4.2 ISED ICES-003 Issue 7 Compliance Declaration
This device was originally tested to the requirements of ICES-003 Issue 6, Information Technology Equipment (Including
Digital Apparatus) — Limits and Methods of Measurement; and evaluated to the updates published in ICES-003, Issue 7,
Information Technology Equipment (Including Digital Apparatus). Based on this evaluation, this product continues to observe
compliance to the requirements set forth by The Innovation, Science and Economic Development Canada (ISED), and
complies with the updates published in ICES-003, Issue 7, Information Technology Equipment (Including Digital Apparatus).

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