Vocollect H1AVA-10001 VHS H1 device model: AVA 100-01 User Manual CERTIFICATE OF COMPLIANCE
Vocollect Inc VHS H1 device model: AVA 100-01 CERTIFICATE OF COMPLIANCE
User Manual
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| Document ID | 848398 |
| Application ID | WNPUvqv0YP4IMx39Stnjgg== |
| Document Description | User Manual |
| Short Term Confidential | No |
| Permanent Confidential | No |
| Supercede | No |
| Document Type | User Manual |
| Display Format | Adobe Acrobat PDF - pdf |
| Filesize | 20.4kB (254992 bits) |
| Date Submitted | 2007-09-27 00:00:00 |
| Date Available | 2007-09-29 00:00:00 |
| Creation Date | 2007-09-26 10:35:37 |
| Producing Software | Acrobat Distiller 7.0.5 (Windows) |
| Document Lastmod | 2007-09-27 09:53:56 |
| Document Title | CERTIFICATE OF COMPLIANCE |
| Document Creator | Acrobat PDFMaker 7.0.7 for Word |
| Document Author: | Systems Administrator |
Rhein Tech Laboratories, Inc. 360 Herndon Parkway Suite 1400 Herndon, VA 20170 http://www.rheintech.com Appendix J: Client: Model #: Standards: ID’s: Report #: Vocollect, Inc. AVA-100-01 FCC 15.247 & RSS-210 MQOH1AVA-10001/2570A-H1AVA101 2007241 Manual Please refer to the following page. Page 47 of 66 Version and Compliance Information: Model Number H1 AVA 100-01 Note: This document contains information about Vocollect Healthcare Systems AccuNurse® Voice Assistant™ H1 device. • Version • Regulatory Policy Compliance AccuNurse Voice Assistant H1 Device Federal Communications Commission Compliance • Specific Absorption Rate (SAR) Level – VHS H1 Device Version For version information, please consult the About page in the AccuNurse Web application. Software AccuNurse Version AccuNurse Voice Assistant H1 Software Consult the release notes. Regulatory Policy Compliance AccuNurse Voice Assistant H1 Federal Communications Commission Compliance This device complies with Part 15 (b) of the Federal Communications Commission (FCC) Rules. Revision 3 September 24, 2007 Specific Absorption Rate (SAR) Level – VHS H1 Device The AccuNurse Voice Assistant H1 with the SDC MCF10G radio has been SAR tested. The maximum SAR value measured was 0.484 W/kg. This product has been tested to the following standards: Standard FCC Part 15, Class B: United States/Federal Communications Commission Code of Federal Regulations, Title 47 Telecommunication Part 15‐Radio Frequency Devices Canada/Industry Canada RSS‐210: Low‐power License‐exempt Radio Communication Devices (All Frequency Bands) Category | Equipment The H1 product may contain one of these radio devices. See device label. Card Manufacturer and P/N AccuNurse Voice Assistant H1 FCC ID # AccuNurse Voice Assistant H1 Industry Canada ID # Summit SDC‐MCF10G MQOH1AVA‐10001 2570A‐H1AVA101 The VHS H1 product is separately approved for: 1. FCC Part 15 Subpart C 2. Industry Canada RSS210 and RSS139 The VHS H1 is nominally a Class B digital device, pursuant to Part 15 of the FCC Rules Revision 3 September 24, 2007 Caution: Exposure to Radio Frequency Radiation The AccuNurse Voice Assistant H1 device contains an internal low‐power radio. The radiated output power of the radio is far below the FCC radio frequency exposure limits. Nevertheless, the device shall be used in such a manner that the potential for human contact with the radio antenna during normal operation is minimized. The device should not be used if the case is open or if the internal antenna is exposed. The device should be worn in accordance with the instructions for this device. VHS devices are designed to be compliant with the rules and regulations in the locations into which they are sold and are labeled as required. VHS devices are type approved and do not require the user to obtain license or authorization before using them. Changes or modifications not expressly approved by Vocollect Healthcare Systems, Inc., could void the userʹs authority to operate the equipment. This Class B digital apparatus complies with Canadian ICES‐003. Cet appareil numérique de la classes B est conforme à la norme NMB‐003 du Canada. Warning: The AccuNurse Voice Assistant H1 device is a class B product. In a domestic environment, this product may cause radio interference in which case the user may be required to take adequate measures. Part 15 (b) of the Federal Communications Commission (FCC) Rules 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. Note: 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 Made in the U.S.A. Revision 3 Vocollect Healthcare Systems, Inc. Pittsburgh, PA September 24, 2007
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