EN55011, 60601-1-2 CE VoC

VERIFICATION OF COMPLIANCE
This Verification of Compliance is hereby issued to the product
designated below.
Product
DC to DC Converter
Model
MIDR03M Series, MIDER03-HI Series
Brand
Applicant
MINMAX TECHNOLOGY CO., LTD.
No. 18, Sin-Sin Road, An-Ping Industrial District, Tainan, 702,
Taiwan, R.O.C
Manufacturer
MINMAX TECHNOLOGY CO., LTD.
No. 18, Sin-Sin Road, An-Ping Industrial District, Tainan, 702,
Taiwan, R.O.C
Applicable Standard(s) EN 55011: 2009+A1: 2010
EN 60601-1-2: 2007+AC: 2010
IEC 61000-4-2: 2008
IEC 61000-4-3: 2010
IEC 61000-4-4: 2012
IEC 61000-4-5: 2014
IEC 61000-4-6: 2013
IEC 61000-4-8: 2009
Reference No.
T150817N11-E1
Test Laboratory
Compliance Certification Services Inc. (Tainan Lab.)
No.8,Jiucengling, Xinhua Dist., Tainan City 712, Taiwan (R.O.C.)
This device has been tested and found to comply with the stated standard(s), which is (are)
required by the Council Directive of 93/42/EEC, 2004/108/EC* and 2014/30/EU, Amended
by 92/31/EEC, 2006/95/EC & 98/13/EC. The test results are indicated in the test report
and are applicable only to the tested sample identified in the report.
Note: The above EN basic standards are applied with latest version if customer has no
special requirement. *: Directive 2004/108/EC is repealed with effect from 20 April 2016.
Jeter Wu / Assistant Manager
Tainan Lab.
Date: September 8, 2015
EC-Declaration of Conformity
The following equipment:
DC to DC Converter
( Product Name )
MIDR03M Series, MIDER03-HI Series /
( Model Designation / Brand Name )
MINMAX TECHNOLOGY CO., LTD.
( Manufacturer Name )
No. 18, Sin-Sin Road, An-Ping Industrial District, Tainan, 702, Taiwan, R.O.C
( Manufacturer Address )
is hereby confirmed to comply with the requirements set out in the Council Directive on
the Approximation of the Laws of the Member States relating to Electromagnetic
Compatibility Directive & Medical Devices (93/42/EEC, 2004/108/EC* and
2014/30/EU, Amended by 92/31/EEC, 2006/95/EC & 98/13/EC (*: Directive
2004/108/EC is repealed with effect from 20 April 2016)). For the evaluation regarding
the Electromagnetic Compatibility & Medical (93/42/EEC, 2004/108/EC and
2014/30/EU, Amended by 92/31/EEC, 2006/95/EC & 98/13/EC) the following
standards are applied:
EN 55011: 2009+A1: 2010
EN 60601-1-2: 2007+AC: 2010
IEC 61000-4-2: 2008
IEC 61000-4-3: 2010
IEC 61000-4-4: 2012
IEC 61000-4-5: 2014
IEC 61000-4-6: 2013
IEC 61000-4-8: 2009
The following manufacturer / importer or authorized representative established within
the EUT is responsible for this declaration:
( Company Name )
( Company Address )
Person responsible for making this declaration:
( Name, Surname )
( Position / Title )
( Place )
( Date )
( Legal Signature )