FCC ID W3L4713809663050
ECG Pen
by MD Biomedical, Inc.
Grantee Code: W3L Product Code: 4713809663050
Latest application date: 2019-12-12
FCC ID Device Details
| FCC ID | W3L4713809663050 |
|---|---|
| Mirrors | fcc.id | gov | fccid.ai |
| Grantee Code | W3L |
| Product Code | 4713809663050 |
| Applicant Business | MD Biomedical, Inc. 🇹🇼 |
| Related Domains |  mdbiomedical.com |
| Equipment Class | ECG Pen |
| Test Firm | Audix Technology Corporation |
Linked Records
Barcode records decoded from published FCC label exhibits or linked by an explicit FCC ID reference on a product page.
| UPC / GTIN | Linked product |
|---|---|
| 4713809663050 EAN-13 · GTIN-14 04713809663050 | ECG Pen 4713809663050 Brand: MD Biomedical, Inc. · Model: 4713809663050 Source: FCC label |
Operating Frequencies
| Frequency Range | Application Purpose | Final Action Date |
|---|---|---|
| 2402-2480 MHz | Original Equipment | 2019-12-12 |
Exhibits
| Document | Type | Available | File |
|---|---|---|---|
| User Manual | Users Manual | 2019-12-12 | PDF 2.1 MB |
| EUT Internal Photo Rev01-1211 | Internal Photos | 2019-12-12 | PDF 5.2 MB |
| EUT External Photo | External Photos | 2019-12-12 | PDF 1.5 MB |
| Label Format and Location | ID Label/Location Info | 2019-12-12 | PDF 88.9 KB |
| Test Setup Photo | Test Setup Photos | 2019-12-12 | PDF 1 MB |
| Test Report | Test Report | 2019-12-12 | PDF 1.8 MB |
| FCC-Application-Form-Authority-Letter | Cover Letter(s) | 2019-12-12 | PDF 279.6 KB |
| FCC-Application-Form-Request for Confidentiality | Cover Letter(s) | 2019-12-12 | PDF 289.6 KB |
| Family model declaration letter | Cover Letter(s) | 2019-12-12 | PDF 230.6 KB |
| FCC-SAR Test Exclusion Evaluation Rev01-1211 | RF Exposure Info | 2019-12-12 | PDF 386.5 KB |
| Block Diagram-870E Metadata only | Block Diagram | PDF 21 KB | |
| Block Diagram-880E Metadata only | Block Diagram | PDF 64.6 KB | |
| Schematic-Module Metadata only | Schematics | PDF 50 KB | |
| Schematic-System-870E Metadata only | Schematics | PDF 54.6 KB | |
| Schematic-System-880E Metadata only | Schematics | PDF 587 KB | |
| Antenna Information Metadata only | Operational Description | PDF 328.9 KB | |
| Operational Description Rev01-1211 Metadata only | Operational Description | PDF 201.3 KB |
Application Information
| Application ID | XRJCAqin5cJkswqxAboOtA== |
|---|---|
| Final Action Date | 2019-12-12 |
| Application Purpose | Original Equipment |
| Applicant FRN | 0018430512 |
| Model | 4713809663050 |
| Frequency Range | 2402-2480 MHz |
| Equipment Class | DTS - Digital Transmission System |
| Device Description | ECG Pen |
| Responsible Party | Rebecca Lin, rebecca.lin@mdbiomedical.com , 886-2-2880-5558 |
| Technical Contact | Ben Cheng, AUDIX Technology Corporation, ben_cheng@audixtech.com  |
| Test Firm | Allen Wang, Audix Technology Corporation, allen_wang@audixtech.com , 886226092133 |
| TCB Email | hotline@acbcert.com  |
| TCB Scope | A4: UNII devices & low power transmitters using spread spectrum techniques |
| Short-Term Confidentiality | No |
| Long-Term Confidentiality | Yes |
| Grant Deferral | No |
| Modular Equipment | Does not apply |
| Composite Device | No |
| 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 output is conducted. This filing meets the SAR threshold exclusion set forth in KDB447498 and therefore can be used in mobile/portable configurations. End-users and installers must be provided with transmitter operating conditions for satisfying RF exposure compliance. |
Applications
| Application ID | Date | Purpose |
|---|---|---|
| XRJCAqin5cJkswqxAboOtA== | 2019-12-12 | Original Equipment |
Equipment Authorization
| Frequency | Output | Rules |
|---|---|---|
| 2402-2480 MHz | 0.0030000 | 15C |
Grants
TCB Grant - Application XRJCAqin5cJkswqxAboOtA==
| TCB | GRANT OF EQUIPMENT AUTHORIZATION |
TCB |
| Certification | ||
| Issued Under the Authority of the | ||
| Federal Communications Commission | ||
| By: |
|
ACB, Inc. 6731 Whittier Avenue Suite C110 McLean, VA 22101 |
Date of Grant: 12/12/2019 Application Dated: 12/11/2019 |
| MD Biomedical, Inc. |
| 8F., No.222, Sec 4, Chengde Rd. |
| Taipei, 111 Taiwan |
| Attention: Rebecca Lin |
| 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: | W3L4713809663050 |
| Name of Grantee: | MD Biomedical, Inc. |
| Equipment Class: | Digital Transmission System |
| Notes: | ECG Pen |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| 15C | 2402.0 - 2480.0 | 0.003 |
| Power output is conducted. This filing meets the SAR threshold exclusion set forth in KDB447498 and therefore can be used in mobile/portable configurations. End-users and installers must be provided with transmitter operating conditions for satisfying RF exposure compliance. |
EAS Grant - Application XRJCAqin5cJkswqxAboOtA==
| COPY |
FEDERAL COMMUNICATIONS COMMISSION WASHINGTON, D.C. 20554 GRANT OF EQUIPMENT AUTHORIZATION |
COPY |
| Certification |
|
MD Biomedical, Inc. 8F., No.222, Sec 4, Chengde Rd. Taipei, 111 Taiwan |
Date of Grant: 12/12/2019 Application Dated: 12/11/2019 |
| Attention: Rebecca Lin |
| 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: | W3L4713809663050 |
| Name of Grantee: | MD Biomedical, Inc. |
| Equipment Class: | Digital Transmission System |
| Notes: | ECG Pen |
| Modular Type: | Does not apply |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| 15C | 2402.0 - 2480.0 | 0.003 |
| Power output is conducted. This filing meets the SAR threshold exclusion set forth in KDB447498 and therefore can be used in mobile/portable configurations. End-users and installers must be provided with transmitter operating conditions for satisfying RF exposure compliance. |
| Mail To: |