ZAWAWireless USB Dongle

This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions: (1) this device may not causeharmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation. Hanges or modifications not expressly approved by the party responsible for compliance could void the user's authority to operate the equipment. 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 radio/TV technician for help.

Advent Medical Products Date:2011-02-18 To: Federal Communications Commission 7435 Oakland Mills Road Columbia, MD FCC ID:ZAWA To Whom It May Concern: This letter is to ascertain that Advent Medical Products. Product Wireless USB Dongle has been the units used for conducting FCC compliance testing, the DoC part will be tested by FCC recognized test lab. If you have any question or concerns, pls. contact us. Sincerely, (Tel)：781-257-5172 E-mail： [email protected] 邮编 ： 01803 Fax: 781-272-4744 Date: February 18, 2011

2206 Ringwood Avenue San Jose, CA 95131 Tel: 408-526-1188 Fax: 408-526-1088 Email: [email protected] Project and Product Certification Representative Authorization Letter Reason for Amendment (current / obsolete) Revision History Approved Date From To Initial Release (current) 1.0 1.0 Revised wording (current) 1.0 2.0 SCS-F18: Project and Product Certification Representative Authorization Letter Page 1 of 2 Rev 2.0 SCS-F18: Project and Product Certification Representative Authorization Letter Page 2 of 2 Rev 2.0 Advent Medical Products February 22, 2011 To: SIEMIC, INC. 2206 Ringwood Avenue, San Jose, CA 95131 USA Dear Sir/Madam, Re: Project and Product Certification Representative Authorization Letter We, Advent Medical Products hereby authorize SIEMIC, INC. to act as a Certification Body for certifying for the following project(s): (Wireless USB Dongle) N/N: TR102 FCC ID: ZAWA We affirm that between SIEMIC and GUANGDONG ROULE ELECTRONICS CO., LTD , any difference in understanding, including test plan, measurement methods, applicable standards and relevant procedures and processes have been resolved prior to commencement of testing activities.

Advent Medical Products Date: April 12, 2011 Federal Communications Commission 7435 Oakland Mills Road Columbia MD 21046 Subject:Request for Confidentiality about date confidential issue, we decide to apply for patent after getting FCC ID certificates we did not aware of this issue when applying . FCC ID: ZAWA To Whom It May Concern: Pursuant to the provisions of Sections 0.457 and 0.459 of the Commission’s rules (47 CFR §§ 0.457, 0.459), we are requesting the Commission to withhold the following attachments as confidential document from public disclosure indefinitely. - Block Diagram - Schematics - Operational Description Above mentioned document contains detailed system and equipment description are considered as proprietary information in operation of the equipment. The public disclosure of above documents might be harmful to our company and would give competitor an unfair advantage in the market. In additional to above mentioned documents, pursuant to Public Notice DA 04-1705 of the Commission’s policy, in order to comply with the marketing regulations in 47 CFR §2.803 and the importation rules in 47 CFR §2.1204, while ensuring that business sensitive information remains confidential until the actual marketing of newly authorized devices. We are requesting the commission to grant short-term confidentiality request on the following attachments until August 23,2011 -Internal Photos -User manual It is our understanding that all measurement test reports, FCC ID label format and correspondent during certification review process cannot be granted as confidential documents and those information will be available for public review once the grant of equipment authorization is issued. We decide to apply for confidentiality now, after getting FCC ID certificates because we were not aware of this issue when applying for Certificate." Signature Best Regards Name : Randall Fincke Title: President Company Name: Advent Medical Products Address: 87 Cambridge St., Burlington, Ma 01803, USA Email: [email protected] Telephone: 781-257-5172

FCC ID label: FCC ID: ZAWA

2 1 FCC ID Location A DO NOT SCALE DRAWING 1400-3022-D_2 SHEET 2 OF 2 8/17/10 EMG UNLESS OTHERWISE SPECIFIED: SCALE: 2:1 WEIGHT: REV DWG. NO. A AAA SIZE TITLE: Advent Medical Products NAME DATE COMMENTS:Q.A. MFG APPR. ENG APPR. CHECKED DRAWN FINISH 3 BEND MATERIAL 5 PROPRIETARY AND CONFIDENTIAL PROPRIETARY AND CONFIDENTIALPROPRIETARY AND CONFIDENTIALPROPRIETARY AND CONFIDENTIAL PROHIBITED. INTERPRET GEOMETRIC TWO PLACE DECIMAL THREE PLACE DECIMAL TOLERANCING PER: DIMENSIONS ARE IN MMTOLERANCES:FRACTIONAL .10 ANGULAR: MACH THE INFORMATION CONTAINED IN THISDRAWING IS THE SOLE PROPERTY OFAdvent Medical Products. ANY REPRODUCTION IN PART OR AS A WHOLEWITHOUT THE WRITTEN PERMISSION OFAdvent Medical Products IS 4 FCC ID Location

Report No.: A001P110113004E Page 1 of 16 FCC TEST REPORT for Advent Medical Products Wireless USB Dongle Model No. : TR102 FCC ID : ZAWA Operating Frequency : 2425-2480 MHz Applicant : Advent Medical Products 87 Cambridge St., Burlington, Ma 01803 USA Regulation : FCC Part 15.249 Subpart C Prepared by : Shenzhen AOV Testing Technology Co., Ltd. 2-6/F, No.5, Yuantou lane, Tanglang, Taoyuan Street, Nanshan District, Shenzhen, Guangdong, China Test Date : February 10-17, 2011 Date of Report : February 17, 2011 Report No.: A001P110113004E Page 2 of 16 TABLE OF CONTENT Description Page Test Report Declaration 1. GENERAL INFORMATION .......................................................................................4 1.1 General Information ........................................................................................................ 4 1.2 Test Facility..................................................................................................................... 4 1.3 Test Instrument Used ..................................................................................................... 5 2. POWERLINE CONDUCTED EMISSION TEST .........................................................6 2.1. Test Standard ................................................................................................................. 6 2.2. Limits .............................................................................................................................. 6 2.3. Test Procedure ............................................................................................................... 6 2.4. Test Result...................................................................................................................... 6 3. RADIATION INTERFERENCE ..................................................................................8 3.1. Rules Part No. ................................................................................................................ 8 3.2. Limits .............................................................................................................................. 8 3.3. Test Procedure ............................................................................................................... 8 3.4. Test Result...................................................................................................................... 9 4. BAND EDGE...........................................................................................................12 4.1. Rules Part No. .............................................................................................................. 12 4.2. Limits ............................................................................................................................ 12 4.3. Test Procedure ............................................................................................................. 12 4.4. Test Result....................................................................................................................12 5. ANTENNA REQUIREMENT ....................................................................................15 5. PHOTOGRAPH OF TEST ...........................................................................................16 Report No.: A001P110113004E Page 3 of 16 TEST REPORT DECLARATION Applicant : Advent Medical Products Manufacturer : Advent Medical Products EUT Description : Wireless USB Dongle Test Procedure Used: FCC Part 15.249 Subpart C The E. U. T. listed below has been completed RF testing by Shenzhen AOV Testing Technology Co., Ltd at the test site of Bontek Compliance Testing Laboratory Ltd. And the Interference emissions can pass FCC Part 15 Subpart B Class B limitations. The test configurations and the facility comply with the radiated and AC line conducted test site criteria in ANSI C63.4-2003. Date of Test: February 10-17, 2011 Prepared by: Project Engineer Reviewer : Project Manager Report No.: A001P110113004E Page 4 of 16 1. GENERAL INFORMATION 1.1 General Information Description : Advent Medical Products Number of Channels : 4CH Model No. : TR102 Applicant : Advent Medical Products 87 Cambridge St., Burlington, Ma 01803 USA Manufacturer : Advent Medical Products 87 Cambridge St., Burlington, Ma 01803 USA 1.2 Test Facility Test Firm : Bontek Compliance Testing Laboratory Ltd. Certificated by FCC, Registration No.: 338263 Address : FL.1, Building H-3, Hua Qiao Cheng East Industrial Area Qiaocheng East Road, Nanshan, Shenzhen, P.R.China Tel : 86-755-86337020 Fax : 86-755-86337028 Report No.: A001P110113004E Page 5 of 16 1.3 Test Instrument Used No. Equipment Manufacturer Model No. S/N Calculator date 1. EMI Test Receiver R&S ESCI 100687 2010-11-22 2. EMI Test Receiver R&S FSU BCT-019 2010-11-22 3. Amplifier HP 8447D 1937A02492 2010-11-22 4. TRILOG Broadband Test-Antenna SCHWARZBECK VULB9163 9163-324 2010-11-22 5. Horn Antenna SCHWARZBECK BBHA9120A B08000991-00 01 2010-11-22 6. High Field Biconical Antenna ELECTRO-METRICS EM-6913 166 2010-11-22 7. Log Periodic Antenna ELECTRO-METRICS EM-6950 811 2010-11-22 8. Remote Active Vertical Antenna ELECTRO-METRICS EM-6892 304 2010-11-22 9. Teo Line Single Phase Module SCHWARZBECK NSLK8128 D-69250 2010-11-22 10. Positioning Controller C&C CC-C-1F MF7802113 2010-11-22 11. Triple-Loop Antenna EVERFINE LLA-2 607004 2010-11-22 12. 10dB attenuator SCHWARZBECK MTAIMP-136 R65.90.0001#0 6 2010-11-22 13. PC IBM R50e RDFE7259 N/A Report No.: A001P110113004E Page 6 of 16 2. POWERLINE CONDUCTED EMISSION TEST 2.1.Test Standard 15.207 2.2.Limits Limits (dBV) Frequency MHz Quasi-peak Level Average Level 0.15 ~ 0.50 66 ~ 56* 56 ~ 46* 0.50 ~ 5.00 56 46 5.00 ~ 30.00 60 50 Notes: 1. *Decreasing linearly with logarithm of frequency. 2. The lower limit shall apply at the transition frequencies. 2.3.Test Procedure The EUT is put on the table that is 0.8m high above the ground and at least away from other Metallic surface 0.4m.…

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