documents安卓版破解版
TEST REPORT
IEC60601-14
Medical electric equipment
Part 1-4: General requirements for safety
Collateral Standard: Programmable electrical medical systems
Report reference No.    :
×××
Compiled by (+ signature)    :
   
Reviewed by (+ signature)    :
   
Date of issue    :
Jan 18, 2010
Applicant    :
Address    :
Standard    :
601-1-4
Test Report Form No.    :
I601-1_C/97-04
TRF Originator    :
Underwriters Laboratories Inc.
Master TRF    :
dated 97-04
Copyright blank test report    :
The bodies participating in the Committee of Certification Bodies (CCB).  This report is based on a blank test report that was prepared by KEMA using information obtained from the TRF originator.
Test procedure    :
Test report only
Procedure deviation    :
N/A
Non-standard test method    :
N/A
Type of test object    :
Trademark    :
Model/type reference    :
Manufacturer    :
Address    :

Rating    :

Copy of marking plate
GENERAL INFORMATION
Test item particulars (see also clause 5):
Classification of installation and use    :
Transportable and portable
Supply connection    :
Non-detachable cord
Accessories and detachables parts included in the evaluation    :
---
Options included    :
---
Possible test case verdicts:
- test case does not apply to the test object    :N/A
- test object does meet the requirement    :Yes
- test object does not meet the requirement    :No
Abbreviations used in the report:
- normal condition    :N.C.
- single fault condition    :S.F.C.
- operational insulation    :OP
- basic insulation    :BI
- basic insulation between parts of opposite polarity    :BOP
- supplementary insulation    :SI
- double insulation    :DI
- reinforced insulation    :RI
General remarks:
"This report is not valid as a CB Test Report unless appended to a CB Test Certificate issued by a NCB, in accordance with IECEE 02".
"(see Attachment #)" refers to additional information appended to the report.
"(see appended table)" refers to a table appended to the report.
Throughout this report a point is used as the decimal separator.
The tests results presented in this report relate only to the object tested.
This report shall not be reproduced except in full without the written approval of the testing laboratory.
List of test equipment must be kept on file and available for review.
Summary of contents provided on the last page of this report.
General product information and considerations:
The A&J-POCB01 Oxygen Concentrator is intended for use as an oxygen concentrator to provide supplemental low flow oxygen therapy in the home, nursing homes, patient care facilities, etc. The A&J-POCB01 is available by prescription only under the supervision of a physician, and is not intended to support or sustain life.

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