FCC ID QRILUMAXT50
Implantable Cardioverter defibrillator
by BIOTRONIK SE & Co. KG
Grantee Code: QRI Product Code: LUMAXT50
Latest application date: 2012-06-13
FCC ID Device Details
| FCC ID | QRILUMAXT50 |
|---|---|
| Mirrors | fcc.id | gov | fccid.ai |
| Grantee Code | QRI |
| Product Code | LUMAXT50 |
| Applicant Business | BIOTRONIK SE & Co. KG 🇩🇪 |
| Related Domains | |
| Equipment Class | Implantable Cardioverter defibrillator |
| Test Firm | Eurofins Product Service GmbH |
Operating Frequencies
| Frequency Range | Application Purpose | Final Action Date |
|---|---|---|
| 402-405 MHz | Original Equipment | 2012-06-13 |
Exhibits
| Document | Type | Available | File |
|---|---|---|---|
| UserMan | Users Manual | 2012-06-13 | PDF 1 MB |
| ExtPho | External Photos | 2012-06-13 | PDF 337.3 KB |
| LabelLoc | ID Label/Location Info | 2012-06-13 | PDF 400.5 KB |
| LabelSmpl | ID Label/Location Info | 2012-06-13 | PDF 88.3 KB |
| TestSup | Test Setup Photos | 2012-06-13 | PDF 301.9 KB |
| conducted test setup | Test Setup Photos | 2012-06-13 | PDF 238 KB |
| TestRep 15.209 | Test Report | 2012-06-13 | PDF 913.1 KB |
| TestRep 95I | Test Report | 2012-06-13 | PDF 1.1 MB |
| Response to FCC ID: QRILUMAXT50 inquiry | Attestation Statements | 2012-06-13 | PDF 23.8 KB |
| AutLet | Cover Letter(s) | 2012-06-13 | PDF 277.1 KB |
| Revised authorisation letter | Cover Letter(s) | 2012-06-13 | PDF 284.4 KB |
| confidentiality int. photos etc | Cover Letter(s) | 2012-06-13 | PDF 562.5 KB |
| RF Exp Statement | RF Exposure Info | 2012-06-13 | PDF 708 KB |
| RFExp | RF Exposure Info | 2012-06-13 | PDF 1.4 MB |
Application Information
| Application ID | n4u0jr3ocEotNgWKKSodww== |
|---|---|
| Final Action Date | 2012-06-13 |
| Application Purpose | Original Equipment |
| Applicant FRN | 0008008591 |
| Model | LUMAXT50 |
| Frequency Range | 402-405 MHz |
| Equipment Class | TNT - Licensed Non-Broadcast Transmitter Worn on Body |
| Device Description | Implantable Cardioverter defibrillator |
| Responsible Party | Gunnar Boersch, Team Manager Regulatory Affairs, gunnar.boersch@biotronik.com |
| Test Firm | Jorg Kusig, Eurofins Product Service GmbH, joergkusig@eurofins.de |
| Short-Term Confidentiality | No |
| Long-Term Confidentiality | Yes |
| Grant Deferral | No |
| Modular Equipment | Does not apply |
| Composite Device | No |
| Composite Part | Yes |
| 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. |
Applications
| Application ID | Date | Purpose |
|---|---|---|
| n4u0jr3ocEotNgWKKSodww== | 2012-06-13 | Original Equipment |
Equipment Authorization
Grants
TCB Grant - Application n4u0jr3ocEotNgWKKSodww==
This application does not exist.
EAS Grant - Application n4u0jr3ocEotNgWKKSodww==
| COPY |
FEDERAL COMMUNICATIONS COMMISSION WASHINGTON, D.C. 20554 GRANT OF EQUIPMENT AUTHORIZATION |
COPY |
| Certification |
|
BIOTRONIK SE & Co. KG Woermannkehre 1 P.O. Box 470255, Berlin, 12359 Germany |
Date of Grant: 06/13/2012 Application Dated: 03/19/2012 |
| Attention: Gunnar Boersch , Team Manager Regulatory Affairs |
| 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: | QRILUMAXT50 |
| Name of Grantee: | BIOTRONIK SE & Co. KG |
| Equipment Class: | Licensed Non-Broadcast Transmitter Worn on Body |
| Notes: | Implantable Cardioverter defibrillator |
| Modular Type: | Does not apply |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| IT | 95I | 402.0 - 405.0 | 4E-7 | 8.05 PM | 236KF1D |
| Output power is EIRP. |
| IT: | Implanted Transmitter |
| Mail To: |
| Joerg Kusig, Head of Certification Department |
| Eurofins Product Service GmbH |
| Storkower Str. 38c |
| Reichenwalde, 15526 |
| Germany |