Partner with UL Technical Experts during your Transition to IEC 60601 3rd edition

Wherever in the world you are selling medical devices, a test report from UL carries with it the advantage of recognition.  UL technical experts serve on the International Technical Committees that developed IEC 60601-1 3^rd edition, so when you work with UL through the transition, you gain the advantage of working with the global leaders in IEC 60601-1 3rd edition knowledge. 

Transition Dates - IEC 60601 3^rd edition

European Union (EU) General Standard	June 1, 2012
European Union (EU) Particular Standards	Varies*
Canada General Standard	June 1, 2012
Canada Particular Standards	Varies*
United States of America (FDA)	July 1, 2013
Brazil	Jan. 1, 2014
Taiwan, Singapore	Recognize 3rd Edition, no transition date announced
Other Countries	TBD

 *Medical devices that fall within the scope of a particular standard are subject to various dates as noted by the Official Journal of the EU for EU and for Canada, a 3 year transition from the date of publication of the particular standard.

Regulatory News:

• March 2012 - Health Canada sent a letter to manufacturers applying for Canadian medical device license clarifying the approach for devices with and without particular standards since not all particular standards have been harmonized with the 3rd edition of IEC 60601.  It also clarified that compliance with 60601-1-9 is not a requirement for licensing.
• February 2012 - NB-MED issued first draft of "Frequently Asked Questions related to the Implementation of EN 60601-1:2006 with respect to MDD 93/42/EEC"

3rd edition tools:

• *NEW Tool* The ISO 14971 Risk Management Toolbox is now for sale.  Ask for more information - Email:  Medical.Inquiry@ul.com
• See how prepared you are for the transition to IEC 60601 3rd edition.  Try our new online self-assessment tool and download a custom report.
• Are you ready for ISO 14971?  Download the ISO 14971 checklist to find out. 

IEC 60601-1 3rd edition resources 

White Papers, Case Studies & Articles

Complementary with Registration

• *NEW* White Paper:  "Choices - IEC 60601-1 3rd Edition and Component Selection"
• Article "IEC 60601 and Risk Management", Medical Electronics Design (2011)
• Article:  "Auditory Alarm Requirements in IEC 60601-1-8 and Risk Management Considerations", Med-Tech Innovation (2011) 
• Article:  60601-1 Third Edition: Why Management Should Consider Converting Now 
• Q&A with UL:  IEC 60601 3rd edition, Release 2, includes specific information on using Power Supplies in 3rd edition end products
• White Paper:  Home Healthcare Equipment: An Overview
• Industry Report:  A Review of Market Entry Requirements for Risk Management, with Special Emphasis on FDA and ISO 14971 Compliance.
• Industry Report:  Risk Management and Post-Market Surveillance:  FDA Considerations
• Industry Report: Major Regulatory Decisions on the Third Edition of IEC 60601-1 (The 3rd Edition Update: 2010)
• Industry Report:  The 3rd Edition Update: 2008
• Industry Report:  The 3rd Edition Update: 2007
• Article:  "A New Perspective on Medical Devices Certification", MD&DI
• Article:  "Regulatory Strategies for the Third Edition of IEC 60601-1", MD&DI
• Article:  "IEC 60601-1 The Third Edition", Kindly reprinted with permission from the Journal of Medical Device Regulation
• Case Study:  Siemens Magnet Technology Ltd.  - ISO 14971 used in IEC 60601 3rd edition    
• White Paper: Major Regulatory Decisions on the Third Edition of IEC 60601   (2008) 

Useful 3rd edition links (external):

• Link to purchase IEC 60601 Amendment 1 (U.S. DRAFT Version)
• Link to free published document IEC 62348 "Mapping between the clauses of the third edition of IEC 60601-1 and the 1998 edition as amended" 
• "Guidance for the Evaluation of Risk Management in Medical Electrical Equipment" - OD-2044-ED.1.0 covers the use of Risk Management for all medical electrical devices, including power supplies.
• Click here for link to IECEE table showing "Use of collateral standards in the IECEE system for 2nd and 3rd Editions of IEC 60601-1" including Biocompatibility
• Status of the publication and recognition of particular standards in the EU on the CENELEC website.
• Purchase IEC 60601-1:2005
• Purchase ANSI/AAMI ES 60601

UL webpages for 60601 collateral and particular standards:

• IEC UL 60601-1 - General Standard, includes 2nd edition
• IEC 60601-1-2 - EMC
• IEC 60601-1 - Software includes 60601-1-4 2nd edition
• IEC 60601-1-11 - Home Healthcare Equipment
• IEC 60601-2-24 - Infusion Pumps
• ISO 14971 - Risk Management  

Contact UL Health Sciences about 60601 3rd edition:

• Join UL Health Sciences Mailing list - Click here to see a list of archived mailings.
• Join UL Health Sciences LinkedIn Group 
• Contact us - www.ul.com/contact
• Email:  Medical.Inquiry@ul.com
• Quote:  HealthSciencesNA@ul.com
• Movie:  www.ul.com/medical/movie