Iec 606011 compliance documents to evaluate medical electrical equipment to the applicable standards. The iec shall not be held responsible for identifying any or all such patent rights. The following information and document downloads are tools to evaluate medical electrical equipment to the applicable standards. Iec 6060122 aamiiec 6060122 specifies requirements for the safety of high frequency hf surgical equipment and hf surgical accessories used in medical practice. This standard is intended to be read in conjunction with asnzs iec 60601. It is a collateral standard its objective is to specify requirements that are in addition to those of the general standard. As part of your fda submission, you need an accredited laboratory to conduct the iec6060112 testing. The most significant changes from iec 6060112 3rd edition to iec 6060112 4th edition are as follows.
As from 1 january 1997 all iec publications are issued with a designation in the 60000 series. Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories. The international electrotechnical commission iec has released iec 60601 22. Particular requirements for the safety of cardiac defibrillators foreword 1 the iec international electrotechnical commission is a worldwide organization for standardization comprising all national electrotechnical committees iec national committees.
Electrical safety testing is essential to ensure safe operating standards for any product that uses electricity directly or indirectly iec 60601 is a series of technical standards for the safety and essential performance of medical electrical equipment, published by the international electrotechnical commission. With the 3rd edition of iec 6060112 still in use, it is often hard to determine which version of iec 6060112 should be used. Iec6060112 is a collateral standard requiring that emc testing is performed on any electronic medical device. As from 1 january 1997 all iec publications are issued with a designation in the. The international electrotechnical commission iec is the leading global organization that prepares and publishes. This particular standard specifies requirements and tests for the safety of ultrasonic physiotherapy equipment. They are provided for free to aid you in your medical equipment design and development, where this information is most useful. The medical device developers guide to iec 606011 601help. F2 labs can help with your fda medical testing and medical device testing and certification. We have been focusing on ecgekg test solutions compliant with medical standards for years and lately extended to eeg testing and wearable device performance testing for vital signs of ecg, ppg heart rate, spo2 and pwtt. This consolidated version of iec 60529 bears the edition number 2. Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories this part of iec 60601 applies to the basic safety and essential. Although iec 6060122 and iec 60601218 do not require multiple samples to be tested, good design practice would dictate enough samples to provide confidence, which in turn depends on the margin.
Iec 606012 24 standard update requirements presentation. Iec 60601 is a series of technical standards for the safety and essential performance of medical electrical equipment, published by the international electrotechnical commission. Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories american national standard eie c. This standard is identical with, and has been reproduced from iec 6060122, ed. Iec 60601 2 1 and en 60601 2 1 testing applies to the basic safety and essential performance of electron accelerators, hereafter referred to as medical electronic equipment, in the range 1 mev to 50 mev, used for treatment of patients. This document comes with our free notification service, good for the life of the document. Our instrument is work together with electrosurgical unitesu which is not our product. Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories, and is now available on the iec webstore. This document is available in either paper or pdf format. Has the status of a basic safety publication in accordance with iec guide 104. Consolidated editions the iec is now publishing consolidated versions of its publications. It amends and supplements iec 606011 second edition, 1988 including amendments 1 and 2, hereinafter referred to as the general standard.
What types of standards are established by iec 60601. Or download the pdf of the directive or of the official journal for free. An expert discusses what medical device manufacturers need to keep in mind as the compliance date for the fourth edition of the iec 6060112 standard approaches. The international electrotechnical commission iec is the leading global organization that prepares and publishes international standards for all electrical, electronic and related technologies. The international electrotechnical commission iec has released iec 6060122. Iec 60601 is a series of technical standards for the safety and essential performance of. Meca 6060180601 medical standards project scope tool. Bs en 6060112 is part of a series of international standards on medical electrical equipment, covering basic safety and essential performance for both equipment and systems. Medical device iec 6060112 emc testing lab sunfire testing. This particular standard amends and supplements iec 606011 third edition, 2005. Particular requirements for the safety of high frequency surgical. En iec 6060122 may 1, 2018 medical electrical equipment part 22. Click here to get our 5 tips for your iec 60601 submission. This standard pertains to medical electrical equipment part 22.
First published in 1977 and regularly updated and restructured, as of 2011 it consists of a general standard, about 10 collateral standards, and about 80 particular standards. Cenelec en iec 6060122 medical electrical equipment. Meca 6060180601 medical standards project scope tool reference only, revision 20150817 check for the latest revision, free to download at. Some lowpowered high frequency surgical equipment for example for microcoagulation, or for use in dentistry or ophthalmology is exempt from certain requirements of this. Particular requirements for the basic safety and essential. This particular standard takes into account iec 6060112 and iec 61689. Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories the new edition 6.
Whaleteq provides the test solutions which assist you to validate and verify your product design with ease. Because insulation thickness varies considerably in normal wiring, it is possible that one sample may pass while another may not. This third edition of iec 6060122 cancels and replaces the second edition published. Our book servers spans in multiple countries, allowing you to get the most less latency time to download any of our books like this one. In order to compliance to the emc requirement, do we need to perform iec 6060112 emc test. Esu testing iec 6060122 electromagnetism electricity scribd. For example, iec 341 is now referred to as iec 600341. Particular requirements for the basic safety and essential performance of medical beds. International standard iec 6060122 has been prepared by subcommittee 62d. Shortwave therapy equipment are defined as medical equipment for the therapeutic treatment of a patient by exposure to electric or magnetic fields produced in the frequency range of more than mhz but not exceeding 45 mhz.
The minimum safety requirements specified in this particular standard are considered to provide for a practical degree of safety in. The author thanks the international electrotechnical commission iec. Hf surgical equipment having a rated output power not exceeding 50 w for example for microcoagulation, or for use in dentistry or ophthalmology is exempt from certain of the requirements of this particular standard. Particular requirements for the basic safety and essential performance.