FCC ID 2BD8CBM1000
Pulse Oximeter
by Shenzhen D-Health Medical Technology Co., Ltd.
Grantee Code: 2BD8C Product Code: BM1000
Latest application date: 2024-01-04
FCC ID Device Details
| FCC ID | 2BD8CBM1000 |
|---|---|
| Mirrors | fcc.id | gov | fccid.ai |
| Grantee Code | 2BD8C |
| Product Code | BM1000 |
| Applicant Business | Shenzhen D-Health Medical Technology Co., Ltd. 🇨🇳 |
| Related Domains |  shberrymed.com |
| Equipment Class | Pulse Oximeter |
| Test Firm | CVC Testing Technology Co., Ltd. |
Operating Frequencies
| Frequency Range | Application Purpose | Final Action Date |
|---|---|---|
| 699-716 MHz | Original Equipment | 2024-01-04 |
Exhibits
| Document | Type | Available | File |
|---|---|---|---|
| User manual | Users Manual | 2024-07-02 | PDF 3.4 MB |
| Internal photos | Internal Photos | 2024-07-02 | PDF 4.8 MB |
| External photos | External Photos | 2024-07-02 | PDF 991.7 KB |
| Label | ID Label/Location Info | 2024-01-04 | PDF 1.9 MB |
| SAR test setup | Test Setup Photos | 2024-07-02 | PDF 155.1 KB |
| Test setup | Test Setup Photos | 2024-07-02 | PDF 728.7 KB |
| Antenna specification | Test Report | 2024-01-04 | PDF 522.8 KB |
| SAR test report | RF Exposure Info | 2024-01-04 | PDF 5.2 MB |
| Test report part 1 | Test Report | 2024-01-04 | PDF 5.9 MB |
| Test report part 2 | Test Report | 2024-01-04 | PDF 4.9 MB |
| Test report part 3 | Test Report | 2024-01-04 | PDF 4.4 MB |
| Test report part 4 | Test Report | 2024-01-04 | PDF 3.6 MB |
| Covered equipment list attestation | Attestation Statements | 2024-01-04 | PDF 30.2 KB |
| US agent attestation | Attestation Statements | 2024-01-04 | PDF 658.4 KB |
| Confidentiality request letter | Cover Letter(s) | 2024-01-04 | PDF 531 KB |
| Block Diagram Metadata only | Block Diagram | PDF 74.9 KB | |
| Schematics Metadata only | Schematics | PDF 163.6 KB | |
| Operational Description Metadata only | Operational Description | PDF 244 KB | |
| Parts list Metadata only | Parts List/Tune Up Info | PDF 114.7 KB | |
| Tune up Metadata only | Parts List/Tune Up Info | PDF 79.1 KB |
Application Information
| Application ID | BFTqV5uuXrbjzIWnnV7DVw== |
|---|---|
| Final Action Date | 2024-01-04 |
| Application Purpose | Original Equipment |
| Applicant FRN | 0034641100 |
| Model | BM1000 |
| Frequency Range | 699-716 MHz |
| Equipment Class | PCB - PCS Licensed Transmitter |
| Device Description | Pulse Oximeter |
| Responsible Party | Xu Yan, Regulatory Affairs Manager, yanxu@shberrymed.com , +8618697555528 |
| Test Firm | Lai Wenjing, CVC Testing Technology Co., Ltd., qt@cvc.org.cn  , 86 2032293684 |
| TCB Email | vina.kerai@nemko.com  |
| TCB Scope | B1: Commercial mobile radio services equipment in the following 47 CFR Parts 20, 22 (cellular), 24,25 (below 3 GHz) & 27 |
| Short-Term Confidentiality | Yes |
| Short-Term Confidentiality Date | 07/02/2024 |
| 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 | Output Power is EIRP and ERP for above and below 1 GHz, respectively. The highest reported SAR for body and extremity (hand) exposure conditions are 1.54 W/kg and 0.83 W/kg, respectively. End-users must be informed of the operating requirements for satisfying RF exposure compliance. This device contains functions that are not operational in the U.S. Territories. This filing is only applicable for U.S. operations. |
Applications
| Application ID | Date | Purpose |
|---|---|---|
| BFTqV5uuXrbjzIWnnV7DVw== | 2024-01-04 | Original Equipment |
Equipment Authorization
Grants
TCB Grant - Application BFTqV5uuXrbjzIWnnV7DVw==
| TCB | GRANT OF EQUIPMENT AUTHORIZATION |
TCB |
| Certification | ||
| Issued Under the Authority of the | ||
| Federal Communications Commission | ||
| By: |
|
Nemko North America, Inc. 303 River Road Ottawa, Ontario, K1V 1H2 Canada |
Date of Grant: 01/04/2024 Application Dated: 01/04/2024 |
| Shenzhen D-Health Medical Technology Co., Ltd. |
| Unit 501, No. 1 Juyin Technology Industrial Plant |
| Jihua Street, Longgang District |
| Shenzhen, 518112 China |
| Attention: Xu Yan , Regulatory Affairs Manager |
| 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: | 2BD8CBM1000 |
| Name of Grantee: | Shenzhen D-Health Medical Technology Co., Ltd. |
| Equipment Class: | PCS Licensed Transmitter |
| Notes: | Pulse Oximeter |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| 24E | 1850.0 - 1910.0 | 0.2871 | 1.0 PM | 1M13G7D | |
| 24E | 1850.0 - 1910.0 | 0.2535 | 1.0 PM | 951KW7D | |
| 27 | 699.0 - 716.0 | 0.0403 | 1.0 PM | 1M12G7D | |
| 27 | 699.0 - 716.0 | 0.039 | 1.0 PM | 943KW7D |
| Output Power is EIRP and ERP for above and below 1 GHz, respectively. The highest reported SAR for body and extremity (hand) exposure conditions are 1.54 W/kg and 0.83 W/kg, respectively. End-users must be informed of the operating requirements for satisfying RF exposure compliance. This device contains functions that are not operational in the U.S. Territories. This filing is only applicable for U.S. operations. |
EAS Grant - Application BFTqV5uuXrbjzIWnnV7DVw==
| COPY |
FEDERAL COMMUNICATIONS COMMISSION WASHINGTON, D.C. 20554 GRANT OF EQUIPMENT AUTHORIZATION |
COPY |
| Certification |
|
Shenzhen D-Health Medical Technology Co., Ltd. Unit 501, No. 1 Juyin Technology Industrial Plant Jihua Street, Longgang District Shenzhen, 518112 China |
Date of Grant: 01/04/2024 Application Dated: 01/04/2024 |
| Attention: Xu Yan , Regulatory Affairs Manager |
| 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: | 2BD8CBM1000 |
| Name of Grantee: | Shenzhen D-Health Medical Technology Co., Ltd. |
| Equipment Class: | PCS Licensed Transmitter |
| Notes: | Pulse Oximeter |
| Modular Type: | Does not apply |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| 24E | 1850.0 - 1910.0 | 0.2871 | 1.0 PM | 1M13G7D | |
| 24E | 1850.0 - 1910.0 | 0.2535 | 1.0 PM | 951KW7D | |
| 27 | 699.0 - 716.0 | 0.0403 | 1.0 PM | 1M12G7D | |
| 27 | 699.0 - 716.0 | 0.039 | 1.0 PM | 943KW7D |
| Output Power is EIRP and ERP for above and below 1 GHz, respectively. The highest reported SAR for body and extremity (hand) exposure conditions are 1.54 W/kg and 0.83 W/kg, respectively. End-users must be informed of the operating requirements for satisfying RF exposure compliance. This device contains functions that are not operational in the U.S. Territories. This filing is only applicable for U.S. operations. |
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