FCC ID QRILUMAXT
Implantable Defibrillator
by BIOTRONIK SE & Co. KG
Grantee Code: QRI Product Code: LUMAXT
Latest application date: 2008-07-28
FCC ID Device Details
| FCC ID | QRILUMAXT |
|---|---|
| Mirrors | fcc.id | gov | fccid.ai |
| Grantee Code | QRI |
| Product Code | LUMAXT |
| Applicant Business | BIOTRONIK SE & Co. KG 🇩🇪 |
| Related Domains | |
| Equipment Class | Implantable Defibrillator |
| Test Firm | Eurofins Product Service GmbH |
Operating Frequencies
| Frequency Range | Application Purpose | Final Action Date |
|---|---|---|
| 402-405 MHz | Class II permissive change or modification of presently authorized equipment | 2008-07-28 |
| 402-405 MHz | Original Equipment | 2006-12-05 |
Exhibits
| Document | Type | Available | File |
|---|---|---|---|
| UserMan | Users Manual | 2008-07-28 | PDF 774.9 KB |
| UserMan | Users Manual | 2006-12-05 | PDF 706.6 KB |
| ExtPho | External Photos | 2008-07-28 | PDF 190.5 KB |
| Photos | External Photos | 2006-12-05 | PDF 361.3 KB |
| Loc | ID Label/Location Info | 2008-07-28 | PDF 30.2 KB |
| Smpl | ID Label/Location Info | 2008-07-28 | PDF 2.8 MB |
| Loc | ID Label/Location Info | 2006-12-05 | PDF 50.6 KB |
| Smpl | ID Label/Location Info | 2006-12-05 | PDF 333 KB |
| rev Location | ID Label/Location Info | 2006-12-05 | PDF 34.5 KB |
| Photos | Test Setup Photos | 2006-12-05 | PDF 324.9 KB |
| Liquid400 | Test Report | 2006-12-05 | PDF 7 KB |
| TestRpt1 | Test Report | 2006-12-05 | PDF 1.8 MB |
| TestRpt2 1 | Test Report | 2006-12-05 | PDF 1.2 MB |
| TestRpt2 2 | Test Report | 2006-12-05 | PDF 2.6 MB |
| Cl2pcL | Cover Letter(s) | 2008-07-28 | PDF 56.2 KB |
| ConfiReq | Cover Letter(s) | 2008-07-28 | PDF 61.6 KB |
| ConfiReq Metadata only | Cover Letter(s) | 2006-12-05 | PDF 47.5 KB |
| ConfiReq rev1 Metadata only | Cover Letter(s) | 2006-12-05 | PDF 72.5 KB |
| ConfiReq rev2 Metadata only | Cover Letter(s) | 2006-12-05 | PDF 43.1 KB |
| ConfiReq rev3 | Cover Letter(s) | 2006-12-05 | PDF 57.4 KB |
| answers 1 to 6 | Cover Letter(s) | 2006-12-05 | PDF 13.6 KB |
| RF Exposure | RF Exposure Info | 2006-12-05 | PDF 846.7 KB |
| IntPho rev1 Metadata only | Internal Photos | PDF 592.9 KB | |
| Photos Metadata only | Internal Photos | PDF 256.8 KB | |
| BlkDia Metadata only | Block Diagram | PDF 131.2 KB | |
| Schem Metadata only | Schematics | PDF 1.3 MB | |
| Antennainfo Metadata only | Operational Description | PDF 45.1 KB | |
| OpDes Metadata only | Operational Description | PDF 142.5 KB | |
| PartList Metadata only | Parts List/Tune Up Info | PDF 117.6 KB |
Application Information
| Application ID | BqZxEVdgAMJnuz7DFym2JA== |
|---|---|
| Final Action Date | 2008-07-28 |
| Application Purpose | Class II permissive change or modification of presently authorized equipment |
| Applicant FRN | 0008008591 |
| Model | LUMAXT |
| Frequency Range | 402-405 MHz |
| Equipment Class | TNT - Licensed Non-Broadcast Transmitter Worn on Body |
| Device Description | Implantable Defibrillator |
| Responsible Party | Gunnar Boersch, Team Manager Regulatory Affairs, gunnar.boersch@biotronik.com |
| Technical Contact | Gunnar Gorecki, Biotronik GmbH & Co. KG, gunnar.gorecki@biotronik.com |
| Non-Technical Contact | Gunnar Boersch, Biotronik GmbH & Co. KG, 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 | No |
| Cognitive Radio | No |
| Authorization Waiver | No |
| Authorization Waiver Approved | No |
| Section 5301 Certification | Yes |
| Related OET Knowledge DataBase Inquiry | No |
Applications
| Application ID | Date | Purpose |
|---|---|---|
| BqZxEVdgAMJnuz7DFym2JA== | 2008-07-28 | Class II permissive change or modification of presently authorized equipment |
| p7f4cllmeQQCfGb8QCW/IA== | 2006-12-05 | Original Equipment |
Equipment Authorization
Grants
TCB Grant - Application p7f4cllmeQQCfGb8QCW/IA==
This application does not exist.
EAS Grant - Application p7f4cllmeQQCfGb8QCW/IA==
| 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: 12/05/2006 Application Dated: 09/26/2006 |
| 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: | QRILUMAXT |
| Name of Grantee: | BIOTRONIK SE & Co. KG |
| Equipment Class: | Licensed Non-Broadcast Transmitter Worn on Body |
| Notes: | Implantable 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 | 5E-7 | 40.0 PM | 230KF1D |
| IT: | Implanted Transmitter |
| Mail To: | |||||||||||||||||||||||||||||||||||||||||||||
| Andreas Herrmann, Certification Manager | |||||||||||||||||||||||||||||||||||||||||||||
| ETS Product Service AG | |||||||||||||||||||||||||||||||||||||||||||||
| Storkower Strasse 38C | |||||||||||||||||||||||||||||||||||||||||||||
| Reichenwalde, D-15526 | |||||||||||||||||||||||||||||||||||||||||||||
| Germany | |||||||||||||||||||||||||||||||||||||||||||||
| 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: 07/28/2008 Application Dated: 06/05/2008 |
| 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: | QRILUMAXT |
| Name of Grantee: | BIOTRONIK SE & Co. KG |
| Equipment Class: | Licensed Non-Broadcast Transmitter Worn on Body |
| Notes: | Implantable 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 | 5E-7 | 40.0 PM | 230KF1D |
| IT: | Implanted Transmitter |
| Mail To: |
| Andreas Herrmann, Certification Manager |
| Eurofins ETS Product Service GmbH |
| Storkower Strasse 38c |
| Reichenwalde, D-15526 |
| Germany |