FCC ID 2BD3B13EA2BD3B
In vitro Diagnostic Medical Device
by P4Q Health S.L.U.
Grantee Code: 2BD3B Product Code: 13EA2BD3B
Latest application date: 2024-06-20
FCC ID Device Details
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 |
|---|---|
| 8445982000051 EAN-13 · GTIN-14 08445982000051 | In vitro Diagnostic Medical Device Brand: P4Q Health S.L.U. · Model: 13EA2BD3B Source: FCC label |
| 8445982000075 EAN-13 · GTIN-14 08445982000075 | In vitro Diagnostic Medical Device Brand: P4Q Health S.L.U. · Model: 13EA2BD3B Source: FCC label |
Operating Frequencies
| Frequency Range | Application Purpose | Final Action Date |
|---|---|---|
| 2402-2480 MHz | Original Equipment | 2024-06-20 |
Exhibits
| Document | Type | Available | File |
|---|---|---|---|
| 10-TF011-PIB21001_revDEKRA_Instructions for use_v2 | Users Manual | 2024-12-17 | PDF 558 KB |
| 1-Internal photos_Q1A-DUO-USB | Internal Photos | 2024-12-17 | PDF 1.4 MB |
| 23-Internal photos_Q1A-VIS-USB | Internal Photos | 2024-12-17 | PDF 1.2 MB |
| 2-External photos_Q1A-DUO-USB | External Photos | 2024-12-17 | PDF 563.5 KB |
| 25-External photos_Q1A-VIS-USB | External Photos | 2024-12-17 | PDF 583.9 KB |
| 3-Label_placement_Q1A-DUO-USB | ID Label/Location Info | 2024-06-20 | PDF 77.5 KB |
| 4-Label_placement_Q1A-VIS-USB | ID Label/Location Info | 2024-06-20 | PDF 94 KB |
| 5-Label_design_Q1A-VIS-USB_Q1A-DUO-USB | ID Label/Location Info | 2024-06-20 | PDF 115.9 KB |
| 20-75285RRF.002_photographs | Test Setup Photos | 2024-12-17 | PDF 849.3 KB |
| 19-Radtenna Test Report - Future Electronics - RL-2022-115 | Test Report | 2024-06-20 | PDF 618.9 KB |
| 9-75285RRF.002A2s | Test Report | 2024-06-20 | PDF 3.9 MB |
| 14-FCC US Agent Attestation_signed | Attestation Statements | 2024-06-20 | PDF 113.5 KB |
| 18-FCB045_00 Certifications concerning covered equipment-REV | Attestation Statements | 2024-06-20 | PDF 30.2 KB |
| 0-FCB012_05 FCC Confidentiality Request_v2-s | Cover Letter(s) | 2024-06-20 | PDF 57.1 KB |
| 11-14-Qassay Similarity Statement_v2-s | Cover Letter(s) | 2024-06-20 | PDF 46.7 KB |
| 13-FCB011_02 FCC Agent letter-s | Cover Letter(s) | 2024-06-20 | PDF 41.7 KB |
| 17-FCB034_00 FCC DoC Declaration letter-s | Cover Letter(s) | 2024-06-20 | PDF 32 KB |
| 12-75285RAN.002s - RF Exp FCC | RF Exposure Info | 2024-06-20 | PDF 663.3 KB |
| 22-D024-PIB21001-revE_Block Diagram Description Metadata only | Block Diagram | PDF 515.7 KB | |
| 15-EQ23001_03_RevD (Bat_Dual) Schematic Metadata only | Schematics | PDF 1.1 MB | |
| 16-EQ23001_02_RevD (Bat_WH) Schematic Metadata only | Schematics | PDF 1.1 MB | |
| 21-stm32wba52ce DS14127 Rev 4 - Datasheet Metadata only | Operational Description | PDF 1.9 MB | |
| 7-Technical_Specifications Metadata only | Operational Description | PDF 633.2 KB |
Application Information
| Application ID | 1yUbuYw2cSvy1ARX6GSm3g== |
|---|---|
| Final Action Date | 2024-06-20 |
| Application Purpose | Original Equipment |
| Applicant FRN | 0034401703 |
| Model | 13EA2BD3B |
| Frequency Range | 2402-2480 MHz |
| Equipment Class | DTS - Digital Transmission System |
| Device Description | In vitro Diagnostic Medical Device |
| Responsible Party | Aitor Alapont Echaniz, Mr, aalapont@p4q.com |
| Agent | Alejandro Alejandro Alejandro, Dekra Testing and Certification SAU, alejandro.gasull@dekra.com |
| Test Firm | Rafael Lopez Martin, DEKRA Testing and Certification, S.A.U., rafael.lopez@dekra.com |
| TCB Email | admin.rcb.es@dekra.com |
| TCB Scope | A4: UNII devices & low power transmitters using spread spectrum techniques |
| Short-Term Confidentiality | Yes |
| Short-Term Confidentiality Date | 12/17/2024 |
| 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 listed is conducted. This device meets the SAR Test Exclusion threshold specified in KDB447498 and since then, it is authorized for portable operation |
Applications
| Application ID | Date | Purpose |
|---|---|---|
| 1yUbuYw2cSvy1ARX6GSm3g== | 2024-06-20 | Original Equipment |
Grants
TCB Grant - Application 1yUbuYw2cSvy1ARX6GSm3g==
| TCB | GRANT OF EQUIPMENT AUTHORIZATION |
TCB |
| Certification | ||
| Issued Under the Authority of the | ||
| Federal Communications Commission | ||
| By: |
|
DEKRA Testing and Certification, S.A.U. Parque Tecnologico de Andalucia, Calle Severo Ochoa 2 y 6 Campanillas - Malaga, 29590 Spain |
Date of Grant: 06/20/2024 Application Dated: 06/19/2024 |
| P4Q Health S.L.U. |
| Calle Nuestra Senora de la Guia Numero 19 |
| Alonsotegi, 48810 Spain |
| Attention: Aitor Alapont Echaniz , Mr |
| 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: | 2BD3B13EA2BD3B |
| Name of Grantee: | P4Q Health S.L.U. |
| Equipment Class: | Digital Transmission System |
| Notes: | In vitro Diagnostic Medical Device |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| 15C | 2402.0 - 2480.0 | 0.002042 | |||
| 15C | 2402.0 - 2480.0 | 0.002123 |
| Output power listed is conducted. This device meets the SAR Test Exclusion threshold specified in KDB447498 and since then, it is authorized for portable operation |
EAS Grant - Application 1yUbuYw2cSvy1ARX6GSm3g==
| COPY |
FEDERAL COMMUNICATIONS COMMISSION WASHINGTON, D.C. 20554 GRANT OF EQUIPMENT AUTHORIZATION |
COPY |
| Certification |
|
P4Q Health S.L.U. Calle Nuestra Senora de la Guia Numero 19 Alonsotegi, 48810 Spain |
Date of Grant: 06/20/2024 Application Dated: 06/19/2024 |
| Attention: Aitor Alapont Echaniz , Mr |
| 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: | 2BD3B13EA2BD3B |
| Name of Grantee: | P4Q Health S.L.U. |
| Equipment Class: | Digital Transmission System |
| Notes: | In vitro Diagnostic Medical Device |
| Modular Type: | Does not apply |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| 15C | 2402.0 - 2480.0 | 0.002042 | |||
| 15C | 2402.0 - 2480.0 | 0.002123 |
| Output power listed is conducted. This device meets the SAR Test Exclusion threshold specified in KDB447498 and since then, it is authorized for portable operation |
| Mail To: |