FCC ID PQC-MX40WLAN2
Intellivue MX40 WLAN2 Patient Worn Device
by Philips Medical Systems North America Co.
Grantee Code: PQC Product Code: MX40WLAN2
Latest application date: 2012-04-30
FCC ID Device Details
| FCC ID | PQC-MX40WLAN2 |
|---|---|
| Mirrors | fcc.id | gov | fccid.ai |
| Grantee Code | PQC |
| Product Code | MX40WLAN2 |
| Applicant Business | Philips Medical Systems North America Co. 🇺🇸 |
| Related Domains |  philips.com |
| Equipment Class | Intellivue MX40 WLAN2 Patient Worn Device |
| Test Firm | Compliance Worldwide, Inc. |
Operating Frequencies
| Frequency Range | Application Purpose | Final Action Date |
|---|---|---|
| 2405-2480 MHz | Original Equipment | 2012-04-30 |
| 5180-5320 MHz | Original Equipment | 2012-04-30 |
Exhibits
| Document | Type | Available | File |
|---|---|---|---|
| USERS MANUAL | Users Manual | 2012-04-30 | PDF 2.6 MB |
| INTERNAL PHOTOS | Internal Photos | 2012-06-14 | PDF 524.9 KB |
| EXTERNAL PHOTOS | External Photos | 2012-04-30 | PDF 125.6 KB |
| LABEL COVER LETTER | ID Label/Location Info | 2012-04-30 | PDF 37.1 KB |
| LABEL LOCATION | ID Label/Location Info | 2012-04-30 | PDF 18.6 KB |
| LABEL SAMPLE | ID Label/Location Info | 2012-04-30 | PDF 57.2 KB |
| TEST SETUP PHOTOS | Test Setup Photos | 2012-04-30 | PDF 162.4 KB |
| TEST REPORT | Test Report | 2012-04-30 | PDF 1.3 MB |
| TEST REPORT | Test Report | 2012-04-30 | PDF 4.6 MB |
| TEST REPORT SRR | Test Report | 2012-04-30 | PDF 612.7 KB |
| ADHOC LETTER | Cover Letter(s) | 2012-04-30 | PDF 34.6 KB |
| AUTHORIZATION LETTER | Cover Letter(s) | 2012-04-30 | PDF 30.9 KB |
| CONFIDENTIAL REQUEST LETTER | Cover Letter(s) | 2012-04-30 | PDF 43.4 KB |
| COVER LETTER | Cover Letter(s) | 2012-04-30 | PDF 28.8 KB |
| LABEL COVER LETTER | Cover Letter(s) | 2012-04-30 | PDF 37.1 KB |
| RF EXPOSURE | RF Exposure Info | 2012-04-30 | PDF 162.4 KB |
| RF EXPOSURE | RF Exposure Info | 2012-04-30 | PDF 206.2 KB |
Application Information
| Application ID | cnyqPXCUyAiTPTasXHRA9A== |
|---|---|
| Final Action Date | 2012-04-30 |
| Application Purpose | Original Equipment |
| Applicant FRN | 0004980637 |
| Model | -MX40WLAN2 |
| Frequency Range | 2405-2480 MHz |
| Equipment Class | DTS - Digital Transmission System |
| Device Description | Intellivue MX40 WLAN2 Patient Worn Device |
| Responsible Party | Delroy Smith, Principal Scientist / Project Leader, delroy.smith@philips.com , + 1 978 659 3382 |
| Test Firm | Larry Stillings, Compliance Worldwide, Inc., LStillings@cw-inc.com  , 603-887-3903 |
| TCB Email | TEI@TIMCOENGR.COM  |
| TCB Scope | A4: UNII devices & low power transmitters using spread spectrum techniques |
| Short-Term Confidentiality | Yes |
| Short-Term Confidentiality Date | 06/14/2012 |
| Long-Term Confidentiality | Yes |
| Grant Deferral | No |
| Modular Equipment | Does not apply |
| Composite Device | Yes |
| Composite Part | No |
| Cognitive Radio | No |
| Authorization Waiver | No |
| Authorization Waiver Approved | No |
| Section 5301 Certification | Yes |
| Related OET Knowledge DataBase Inquiry | No |
| Grant Comments | Power listed is conducted. This device is approved for operation in the Wireless Medical Telemetry Service. This device and its antenna(s) must not be co-located or operating in conjunction with any other antenna or transmitter except in accordance with FCC multi-transmitter product procedures. End-users must be provided with specific operating instructions for satisfying RF exposure compliance. |
Applications
| Application ID | Date | Purpose |
|---|---|---|
| cnyqPXCUyAiTPTasXHRA9A== | 2012-04-30 | Original Equipment |
| 9e6o7XrBF17HdivE5eNNEQ== | 2012-04-30 | Original Equipment |
Equipment Authorization
Grants
TCB Grant - Application cnyqPXCUyAiTPTasXHRA9A==
| TCB | GRANT OF EQUIPMENT AUTHORIZATION |
TCB |
| Certification | ||
| Issued Under the Authority of the | ||
| Federal Communications Commission | ||
| By: |
|
Timco Engineering, Inc. 849 NW State Road 45 <BR>P.O. Box 370, Newberry, FL 32669 |
Date of Grant: 04/30/2012 Application Dated: 04/30/2012 |
| Philips Medical Systems North America Co. |
| 3000 Minuteman Road |
| Andover, MA 01810-1099 |
| Attention: Delroy Smith , Principal Scientist / Project Leader |
| NOT TRANSFERABLE |
| EQUIPMENT AUTHORIZATION is hereby issued to the named GRANTEE, and is VALID ONLY for the equipment identified hereon for use under the Commission's Rules and Regulations listed below. |
| FCC IDENTIFIER: | PQC-MX40WLAN2 |
| Name of Grantee: | Philips Medical Systems North America Co. |
| Equipment Class: | Digital Transmission System |
| Notes: | Intellivue MX40 WLAN2 Patient Worn Device |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15C | 2412.0 - 2462.0 | 0.083 | ||
| CC | 15C | 2405.0 - 2480.0 | 0.0006 |
| Power listed is conducted. This device is approved for operation in the Wireless Medical Telemetry Service. This device and its antenna(s) must not be co-located or operating in conjunction with any other antenna or transmitter except in accordance with FCC multi-transmitter product procedures. End-users must be provided with specific operating instructions for satisfying RF exposure compliance. |
| CC: | This device is certified pursuant to two different Part 15 rules sections. |
EAS Grant - Application cnyqPXCUyAiTPTasXHRA9A==
| COPY |
FEDERAL COMMUNICATIONS COMMISSION WASHINGTON, D.C. 20554 GRANT OF EQUIPMENT AUTHORIZATION |
COPY |
| Certification |
|
Philips Medical Systems North America Co. 3000 Minuteman Road Andover, MA 01810-1099 United States |
Date of Grant: 04/30/2012 Application Dated: 04/30/2012 |
| Attention: Delroy Smith , Principal Scientist / Project Leader |
| NOT TRANSFERABLE |
| EQUIPMENT AUTHORIZATION is hereby issued to the named GRANTEE, and is VALID ONLY for the equipment identified hereon for use under the Commission's Rules and Regulations listed below. |
| FCC IDENTIFIER: | PQC-MX40WLAN2 |
| Name of Grantee: | Philips Medical Systems North America Co. |
| Equipment Class: | Digital Transmission System |
| Notes: | Intellivue MX40 WLAN2 Patient Worn Device |
| Modular Type: | Does not apply |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15C | 2412.0 - 2462.0 | 0.083 | ||
| CC | 15C | 2405.0 - 2480.0 | 0.0006 |
| Power listed is conducted. This device is approved for operation in the Wireless Medical Telemetry Service. This device and its antenna(s) must not be co-located or operating in conjunction with any other antenna or transmitter except in accordance with FCC multi-transmitter product procedures. End-users must be provided with specific operating instructions for satisfying RF exposure compliance. |
| CC: | This device is certified pursuant to two different Part 15 rules sections. |
| Mail To: | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| TCB | GRANT OF EQUIPMENT AUTHORIZATION |
TCB |
| Certification | ||
| Issued Under the Authority of the | ||
| Federal Communications Commission | ||
| By: |
|
Timco Engineering, Inc. 849 NW State Road 45 <BR>P.O. Box 370, Newberry, FL 32669 |
Date of Grant: 04/30/2012 Application Dated: 04/30/2012 |
| Philips Medical Systems North America Co. |
| 3000 Minuteman Road |
| Andover, MA 01810-1099 |
| Attention: Delroy Smith , Principal Scientist / Project Leader |
| NOT TRANSFERABLE |
| EQUIPMENT AUTHORIZATION is hereby issued to the named GRANTEE, and is VALID ONLY for the equipment identified hereon for use under the Commission's Rules and Regulations listed below. |
| FCC IDENTIFIER: | PQC-MX40WLAN2 |
| Name of Grantee: | Philips Medical Systems North America Co. |
| Equipment Class: | Unlicensed National Information Infrastructure TX |
| Notes: | INTELLIVUE MX40 WLAN2 PATIENT WORN DEVICE |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15E | 5180.0 - 5320.0 | 0.02245 | ||
| CC | 15E | 5500.0 - 5580.0 | 0.04604 | ||
| CC | 15E | 5660.0 - 5700.0 | 0.04766 | ||
| CC | 15E | 5745.0 - 5805.0 | 0.06655 |
| Power listed is conducted. This device is restricted to indoor use only within the 5150-5250MHz band. This device is approved for operation in the Wireless Medical Telemetry Service. This device and its antenna(s) must not be co-located or operating in conjunction with any other antenna or transmitter except in accordance with FCC multi-transmitter product procedures. End-users must be provided with specific operating instructions for satisfying RF exposure compliance. |
| CC: | This device is certified pursuant to two different Part 15 rules sections. |
EAS Grant - Application 9e6o7XrBF17HdivE5eNNEQ==
| COPY |
FEDERAL COMMUNICATIONS COMMISSION WASHINGTON, D.C. 20554 GRANT OF EQUIPMENT AUTHORIZATION |
COPY |
| Certification |
|
Philips Medical Systems North America Co. 3000 Minuteman Road Andover, MA 01810-1099 United States |
Date of Grant: 04/30/2012 Application Dated: 04/30/2012 |
| Attention: Delroy Smith , Principal Scientist / Project Leader |
| NOT TRANSFERABLE |
| EQUIPMENT AUTHORIZATION is hereby issued to the named GRANTEE, and is VALID ONLY for the equipment identified hereon for use under the Commission's Rules and Regulations listed below. |
| FCC IDENTIFIER: | PQC-MX40WLAN2 |
| Name of Grantee: | Philips Medical Systems North America Co. |
| Equipment Class: | Unlicensed National Information Infrastructure TX |
| Notes: | INTELLIVUE MX40 WLAN2 PATIENT WORN DEVICE |
| Modular Type: | Does not apply |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15E | 5180.0 - 5320.0 | 0.02245 | ||
| CC | 15E | 5500.0 - 5580.0 | 0.04604 | ||
| CC | 15E | 5660.0 - 5700.0 | 0.04766 | ||
| CC | 15E | 5745.0 - 5805.0 | 0.06655 |
| Power listed is conducted. This device is restricted to indoor use only within the 5150-5250MHz band. This device is approved for operation in the Wireless Medical Telemetry Service. This device and its antenna(s) must not be co-located or operating in conjunction with any other antenna or transmitter except in accordance with FCC multi-transmitter product procedures. End-users must be provided with specific operating instructions for satisfying RF exposure compliance. |
| CC: | This device is certified pursuant to two different Part 15 rules sections. |
| Mail To: |