FCC ID PQC-MX40SH1C4
MX40 1.4 GHz CTS Patient Worn Device
by Philips Medical Systems North America Co.
Grantee Code: PQC Product Code: MX40SH1C4
Latest application date: 2022-11-29
FCC ID Device Details
| FCC ID | PQC-MX40SH1C4 |
|---|---|
| Mirrors | fcc.id | gov | fccid.ai |
| Grantee Code | PQC |
| Product Code | MX40SH1C4 |
| Applicant Business | Philips Medical Systems North America Co. 🇺🇸 |
| Related Domains |  philips.com |
| Equipment Class | MX40 1.4 GHz CTS Patient Worn Device |
| Test Firm | Timco Engineering, Inc. |
Operating Frequencies
| Frequency Range | Application Purpose | Final Action Date |
|---|---|---|
| 1391.65 MHz | Class II permissive change or modification of presently authorized equipment | 2022-11-29 |
| 5180-5320 MHz | Original Equipment | 2014-04-01 |
| 2405-2480 MHz | Original Equipment | 2014-04-01 |
| 1395.9-1399.1 MHz | Original Equipment | 2014-04-01 |
Exhibits
| Document | Type | Available | File |
|---|---|---|---|
| USERS MANUAL | Users Manual | 2014-04-01 | PDF 2.7 MB |
| INTERNAL PHOTOS | Internal Photos | 2014-09-28 | PDF 634.4 KB |
| INTERNAL PHOTOS | Internal Photos | 2014-09-28 | PDF 1.9 MB |
| EXTERNAL PHOTOS | External Photos | 2014-04-01 | PDF 231.5 KB |
| LABEL LOCATION | ID Label/Location Info | 2014-04-01 | PDF 1.3 MB |
| LABEL SAMPLE | ID Label/Location Info | 2014-04-01 | PDF 1.3 MB |
| TEST SETUP PHOTOS | Test Setup Photos | 2014-04-01 | PDF 585.6 KB |
| SRR REPORT | Test Report | 2014-04-01 | PDF 498 KB |
| TEST REPORT | Test Report | 2014-04-01 | PDF 1.1 MB |
| TEST REPORT | Test Report | 2014-04-01 | PDF 3.6 MB |
| TEST REPORT | Test Report | 2014-04-01 | PDF 4.2 MB |
| ATTESTATION LETTER | Cover Letter(s) | 2014-04-01 | PDF 40 KB |
| Confidentiality Request | Cover Letter(s) | 2022-11-29 | PDF 98.9 KB |
| c2pc Assertion | Cover Letter(s) | 2022-11-29 | PDF 83 KB |
| c2pc Consent | Cover Letter(s) | 2022-11-29 | PDF 122.9 KB |
| c2pc Cover Letter | Cover Letter(s) | 2022-11-29 | PDF 140.2 KB |
| AUTHORIZATION LETTER | Cover Letter(s) | 2014-04-01 | PDF 33.9 KB |
| CONFIDENTIAL LETTER | Cover Letter(s) | 2014-04-01 | PDF 76.4 KB |
| COVER LETTER FOR LABEL | Cover Letter(s) | 2014-04-01 | PDF 42.1 KB |
| RF EXPOSURE | RF Exposure Info | 2014-04-01 | PDF 185.5 KB |
| RF EXPOSURE | RF Exposure Info | 2014-04-01 | PDF 83.7 KB |
| RF EXPOSURE | RF Exposure Info | 2014-04-01 | PDF 84.8 KB |
| BLOCK DIAGRAM Metadata only | Block Diagram | PDF 33.8 KB | |
| BLOCK DIAGRAM Metadata only | Block Diagram | PDF 140.3 KB | |
| SCHEMATICS Metadata only | Schematics | PDF 170.6 KB | |
| SCHEMATICS Metadata only | Schematics | PDF 118.8 KB | |
| Associated KDB Inquiry and FCC response Metadata only | Operational Description | PDF 18 KB | |
| OPERATIONAL DESCRIPTION Metadata only | Operational Description | PDF 277.8 KB | |
| PARTS LIST Metadata only | Parts List/Tune Up Info | PDF 74.1 KB | |
| PARTS LIST Metadata only | Parts List/Tune Up Info | PDF 73 KB | |
| TUNE UP INFO Metadata only | Parts List/Tune Up Info | PDF 57.9 KB | |
| TUNE UP INFO Metadata only | Parts List/Tune Up Info | PDF 45.8 KB |
Application Information
| Application ID | 7JJJkc92AE5p1C85JxhIsA== |
|---|---|
| Final Action Date | 2022-11-29 |
| Application Purpose | Class II permissive change or modification of presently authorized equipment |
| Applicant FRN | 0004980637 |
| Model | MX40SH1C4 |
| Frequency Range | 1391.65 MHz |
| Equipment Class | TNT - Licensed Non-Broadcast Transmitter Worn on Body |
| Device Description | MX40 1.4 GHz CTS Patient Worn Device |
| Responsible Party | Delroy Smith, Principal Scientist / Project Leader, delroy.smith@philips.com , + 1 978 659 3382 |
| Technical Contact | Delroy Smith, Philps Healthcare, delroy.smith@philips.com , 9784470872 |
| Test Firm | Bruno Clavier, Timco Engineering, Inc., bruno@timcoengr.com  , 352-472-5500 |
| TCB Email | hotline@acbcert.com  |
| TCB Scope | B2: General Mobile Radio And Broadcast Services equipment in the following 47 CFR Parts 22 (non-cellular) 73, 74, 90, 95, 97, & 101 (all below 3 GHz) |
| Short-Term Confidentiality | No |
| 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 | Class II Permissive Change 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 multitransmitter product procedures. End-users must be provided with specific operating instructions for satisfying RF exposure compliance. This c2pc adds Part 27 emission line entries. |
Applications
| Application ID | Date | Purpose |
|---|---|---|
| 7JJJkc92AE5p1C85JxhIsA== | 2022-11-29 | Class II permissive change or modification of presently authorized equipment |
| wfpzdnmw1cBB+GTiVDoRCw== | 2014-04-01 | Original Equipment |
| k1DdiPOHHgCXd6EPQhReWA== | 2014-04-01 | Original Equipment |
| Eqa9tgJUf29rKU6rsd9W2A== | 2014-04-01 | Original Equipment |
Equipment Authorization
| Frequency | Output | Tolerance | Emission | Rules | Grant Notes |
|---|---|---|---|---|---|
| 1391.65 MHz | 0.0035 | 2.5ppm | 1M14G7D | 27 | |
| 1395.9-1399.1 MHz | 0.0035 | 0.00129% | 1M18L7D | 95H | |
| 1427.9-1431.1 MHz | 0.0036 | 0.0009% | 1M18L7D | 95H | |
| 1433.544 MHz | 0.0036 | 2.5ppm | 1M14G7D | 27 | |
| 2405-2480 MHz | 0.0006 | 15C | CC | ||
| 2412-2462 MHz | 0.0832 | 15C | CC | ||
| 5180-5320 MHz | 0.02245 | 15E | CC | ||
| 5500-5580 MHz | 0.04604 | 15E | CC | ||
| 5660-5700 MHz | 0.04766 | 15E | CC | ||
| 5745-5805 MHz | 0.06655 | 15E | CC |
Grants
TCB Grant - Application wfpzdnmw1cBB+GTiVDoRCw==
| 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 Newberry, FL 32669 |
Date of Grant: 04/01/2014 Application Dated: 04/01/2014 |
| 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-MX40SH1C4 |
| Name of Grantee: | Philips Medical Systems North America Co. |
| Equipment Class: | Unlicensed National Information Infrastructure TX |
| Notes: | Intellivue MX40 1.4 GHz 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 wfpzdnmw1cBB+GTiVDoRCw==
| 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: 04/01/2014 Application Dated: 04/01/2014 |
| 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-MX40SH1C4 |
| Name of Grantee: | Philips Medical Systems North America Co. |
| Equipment Class: | Unlicensed National Information Infrastructure TX |
| Notes: | Intellivue MX40 1.4 GHz 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: | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 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 Newberry, FL 32669 |
Date of Grant: 04/01/2014 Application Dated: 04/01/2014 |
| 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-MX40SH1C4 |
| Name of Grantee: | Philips Medical Systems North America Co. |
| Equipment Class: | Digital Transmission System |
| Notes: | Intellivue MX40 1.4 GHz Patient Worn Device |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15C | 2412.0 - 2462.0 | 0.0832 | ||
| 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 k1DdiPOHHgCXd6EPQhReWA==
| 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: 04/01/2014 Application Dated: 04/01/2014 |
| 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-MX40SH1C4 |
| Name of Grantee: | Philips Medical Systems North America Co. |
| Equipment Class: | Digital Transmission System |
| Notes: | Intellivue MX40 1.4 GHz 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 | 0.0832 | ||
| 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 Newberry, FL 32669 |
Date of Grant: 04/01/2014 Application Dated: 04/01/2014 |
| 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-MX40SH1C4 |
| Name of Grantee: | Philips Medical Systems North America Co. |
| Equipment Class: | Licensed Non-Broadcast Transmitter Worn on Body |
| Notes: | MX40 1.4 GHz CTS Patient Worn Device |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| 95H | 1395.9 - 1399.1 | 0.0035 | 0.00129 % | 1M18L7D | |
| 95H | 1427.9 - 1431.1 | 0.0036 | 0.0009 % | 1M18L7D |
| 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. |
EAS Grant - Application Eqa9tgJUf29rKU6rsd9W2A==
| 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: 04/01/2014 Application Dated: 04/01/2014 |
| 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-MX40SH1C4 |
| Name of Grantee: | Philips Medical Systems North America Co. |
| Equipment Class: | Licensed Non-Broadcast Transmitter Worn on Body |
| Notes: | MX40 1.4 GHz CTS Patient Worn Device |
| Modular Type: | Does not apply |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| 95H | 1395.9 - 1399.1 | 0.0035 | 0.00129 % | 1M18L7D | |
| 95H | 1427.9 - 1431.1 | 0.0036 | 0.0009 % | 1M18L7D |
| 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. |
| Mail To: | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| TCB | GRANT OF EQUIPMENT AUTHORIZATION |
TCB |
| Certification | ||
| Issued Under the Authority of the | ||
| Federal Communications Commission | ||
| By: |
|
ACB, Inc. 313 Park Avenue Suite 300 Falls Church, VA 22046 |
Date of Grant: 11/29/2022 Application Dated: 11/29/2022 |
| 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-MX40SH1C4 |
| Name of Grantee: | Philips Medical Systems North America Co. |
| Equipment Class: | Licensed Non-Broadcast Transmitter Worn on Body |
| Notes: | MX40 1.4 GHz CTS Patient Worn Device |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| 95H | 1395.9 - 1399.1 | 0.0035 | 0.00129 % | 1M18L7D | |
| 95H | 1427.9 - 1431.1 | 0.0036 | 0.0009 % | 1M18L7D | |
| 27 | 1391.65 - 1391.65 | 0.0035 | 2.5 PM | 1M14G7D | |
| 27 | 1433.544 - 1433.544 | 0.0036 | 2.5 PM | 1M14G7D |
| Class II Permissive Change 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 multitransmitter product procedures. End-users must be provided with specific operating instructions for satisfying RF exposure compliance. This c2pc adds Part 27 emission line entries. |
EAS Grant - Application 7JJJkc92AE5p1C85JxhIsA==
| 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: 11/29/2022 Application Dated: 11/29/2022 |
| 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-MX40SH1C4 |
| Name of Grantee: | Philips Medical Systems North America Co. |
| Equipment Class: | Licensed Non-Broadcast Transmitter Worn on Body |
| Notes: | MX40 1.4 GHz CTS Patient Worn Device |
| Modular Type: | Does not apply |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| 95H | 1395.9 - 1399.1 | 0.0035 | 0.00129 % | 1M18L7D | |
| 95H | 1427.9 - 1431.1 | 0.0036 | 0.0009 % | 1M18L7D | |
| 27 | 1391.65 - 1391.65 | 0.0035 | 2.5 PM | 1M14G7D | |
| 27 | 1433.544 - 1433.544 | 0.0036 | 2.5 PM | 1M14G7D |
| Class II Permissive Change 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 multitransmitter product procedures. End-users must be provided with specific operating instructions for satisfying RF exposure compliance. This c2pc adds Part 27 emission line entries. |
| Mail To: |