This blog will you understand the definition of Patient Applied Parts for medical electrical equipment under the IEC 60601-1 Standard. This blog discusses the following points: Definition of APPLIED PART Examples of APPLIED PARTS for specific medical devices Examples of different
OSHA to Add AAMI ES 60601-1 to ‘List of Appropriate’ NRTL Program Test Standards
OSHA adding AAMI ES 60601-1 to the ‘List of Appropriate’ NRTL Program Test Standards is discussed in this blog. BIG News!!! News, I have been waiting for many years now is that OSHA, finally, under it’s NRTL (Nationally Recognized Test
Status Update on EN 60601-1:06 + A1:13 for EU MDD & Annexes ZA & ZZ
EN 60601-1 (2006) + A1 (2013) status for EU MDD Harmonization & Impact of Annex ZA & ZZ are discussed in this blog.
IEC 60601 Medical Electrical Equipment Classifications: FAQ’s
IEC 60601 medical electrical equipment classification frequently asked questions are discussed in this blog. Why do I need to classify my product for IEC 60601-1, 3rd ed.? – The standard says you have to classify“…ME EQUIPMENT, or parts thereof, including applied parts…” as
When will FDA Issue Guidance Document on AAMI ES 60601-1, 3rd ed. + Amendment 1?
That’s a really good question and the answer is sooner than I would have thought. Especially since the draft guidance has been pushed forward and then pushed back aside so many times internally at FDA it is really hard to