US medical device regulators have announced more than 30 new additions to their list of recognized device consensus standards.
In a Federal Register announcement on 9 July 2014, the US Food and Drug Administration (FDA) announced its 36th update to its "List of Recognized Standards"—its fourth update to the list in 2014—containing dozens of modifications and 33 newly recognized standards.
Those standards come to be recognized by FDA through a process known as "incorporation by reference." Because the standards are often highly technical, time-consuming to produce and expensive to create, FDA defers to outside technical experts to create the standards, and then adopts those standards—sometimes with changes, but most often without—for use by regulated industry.
Members of industry are then responsible for complying with those standards, and usually must pay to access them.
So far this year, FDA has released three updates to the list of recognized standards:
Those updates have ranged from the minute, such as update 33's five new standards and 35's three new standards, but can also be massive, such as update 34's hundreds of changes and two dozen additions.
FDA's newest Recognition List, number 36, appears to be its largest yet this year, with 33 new standards and 153 changes to existing standards.
All newly-recognized standards may be found below. All other standards can be found in FDA's Federal Register notice.
| Recognition No. | Title of standard | Reference No. and date |
|---|---|---|
| A. Cardiovascular | ||
| 3-127 | Medical electrical equipment—Part 2-47: Particular requirements for the basic safety and essential performance of ambulatory electrocardiographic systems | ANSI/AAMI/IEC 60601-2-47:2012. |
| 3-128 | Active implantable medical devices—Electromagnetic compatibility—EMC test protocols for implantable cardiac pacemakers, implantable cardioverter defibrillators, and cardiac resynchronization devices | ANSI/AAMI/ISO 14117:2012. |
| B. General I (Quality System/Risk Management (QS/RM)) | ||
| 5-89 | Medical electrical equipment—Part 1-6: General requirements for basic safety and essential performance—Collateral standard: Usability | IEC 60601-1-6 Edition 3.1 2013-10. |
| 5-92 | Medical Electrical Equipment—Part 1-8: General requirements for basic safety and essential performance—Collateral standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems | ANSI/AAMI/IEC 60601-1-8:2006 & A1:2012. |
| C. General II (Electrical Safety/Electromagnetic Compatibility (ES/EMC)) | ||
| 19-1 | Medical electrical equipment—Part 1-2: General requirements for basic safety and essential performance—Collateral standard: electromagnetic compatibility—requirements and tests | IEC 60601-1-2 Edition 3:2007-03. |
| 19-2 | Medical electrical equipment—Part 1-2: General requirements for basic safety and essential performance—Collateral standard: electromagnetic compatibility—requirements and tests | ANSI/AAMI/IEC 60601-1-2:2007/(R)2012. |
| 19-3 | Medical electrical equipment—Part 1-10: General requirements for basic safety and essential performance—Collateral standard: requirements for the development of physiologic closed-loop controllers | IEC 60601-1-10 Edition 1.0:2007-11. |
| 19-4 | Medical electrical equipment—Part 1: General requirements for basic safety and essential performance (IEC 60601-1:2005, mod) | ANSI/AAMI ES60601-1:2005/(R)2012 and A1:2012,C1:2009/(R)2012 and A2:2010/(R)2012. |
| 19-5 | Medical electrical equipment—Part 1: General requirements for basic safety and essential performance (IEC 60601-1:2005, mod) | ANSI/AAMI ES60601-1:2005/(R)2012 and C1:2009/(R)2012 and, A2:2010/(R)2012 (Consolidated text). |
| 19-6 | Medical electrical equipment—Part 1-11: General requirements for basic safety and essential performance—Collateral standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment [Including: Technical corrigendum 1 (2011)] | IEC 60601-1-11 Edition 1.0:2010-04. |
| 19-7 | Medical electrical equipment—Part 1-11: General requirements for basic safety and essential performance—Collateral standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment (IEC 60601-1-11:2010 mod) | ANSI/AAMI HA60601-1-11:2011. |
| 19-8 | Medical electrical equipment—Part 1-2: General requirements for basic safety and essential performance—Collateral standard: Electromagnetic disturbances—Requirements and tests | IEC 60601-1-2 Edition 4.0:2014-02. |
| 19-9 | Medical electrical equipment—Part 1-10: General requirements for basic safety and essential performance—Collateral standard: Requirements for the development of physiologic closed-loop controllers | IEC 60601-1-10 Edition 1.1:2013-11. |
| 19-10 | Lithium batteries | UL 1642 5th Edition 2013. |
| 19-11 | Household and commercial batteries | UL 2054 2nd Edition 2011. |
| D. Orthopedics | ||
| 11-279 | Standard practice for finite element analysis (FEA) of non-modular metallic orthopaedic hip femoral stems | ASTM F2996-13. |
| 11-280 | Standard test method for static, dynamic, and wear assessment of extra-discal single level spinal constructs | ASTM F2624-12. |
| E. Radiology | ||
| 12-275 | Ultrasonics—Power measurement—Radiation force balances and performance requirements | IEC 61161 Edition 3.0:2013-01. |
| 12-276 | Ultrasonics—Output test—Guide for the maintenance of ultrasound physiotherapy systems | IEC TS 62462 First edition 2007-05. |
| 12-277 | Ultrasonics—Hydrophones—Part 1: Measurement and characterization of medical ultrasonic fields up to 40 megahertz (MHz) | IEC 62127-1 Edition 1.1:2013-02. |
| 12-278 | Ultrasonics—Hydrophones—Part 2: Calibration for ultrasonic fields up to 40 MHz (including corrigendum 1:2008 and amendment 1:2013) | IEC 62127-2 Edition 1.0:2007-08. |
| 12-279 | Ultrasonics—Hydrophones—Part 3: Properties of hydrophones for ultrasonic fields up to 40 MHz | IEC 62127-3 Edition 1.1:2013-05. |
| 12-280 | Ultrasonics—Power measurement—High intensity therapeutic ultrasound (HITU) transducers and systems | IEC 62555 Edition 1.0:2013-11. |
| 12-281 | Medical electrical equipment—Part 2-62: Particular requirements for the basic safety and essential performance of high intensity therapeutic ultrasound (HITU) equipment | IEC 60601-2-62 Edition 1.0:2013-07. |
| 12-282 | Eyewear for protection against intense light sources used on humans and animals for cosmetic and medical applications—Part 1: Specification for products | ISO 12609-1 First edition 2013-07-15. |
| 12-283 | Eyewear for protection against intense light sources used on humans and animals for cosmetic and medical applications—Part 2: Guidance for use | ISO 12609-2 First edition 2013-07-15. |
| F. Software/Informatics | ||
| 13-67 | Health informatics—Personal health device communication—Part 10418: Device specialization—International normalized ratio (INR) monitor | ISO/IEEE 11073-10418 First edition 2014-03-01. |
| 13-68 | Health informatics—Point-of-care medical device communication—Part 90101: Analytical instruments—Point-of-care test | ISO 11073-90101 First edition 2008-01-15. |
| 13-69 | Health Informatics—Personal health device communication—Part 10472: Device specialization—Medication monitor | ISO/IEEE 11073-10472 First edition 2012-11-01. |
| G. Sterility | ||
| 14-436 | Practice for dosimetry in radiation processing | ISO/ASTM 52628 First edition 2013-11-15. |
| 14-437 | Guide for performance characterization of dosimeters and dosimetry systems for use in radiation processing | ISO/ASTM 52701 First edition 2013-11-15. |
| 14-450 | Biological indicators—Resistance performance tests | USP 37-NF32:2014 <55>. |
| 14-451 | Biological indicators for sterilization | USP 37-NF32:2014 <1035>. |
We have completed our migration to a new platform and are pleased to introduce the updated site.
What to expect: If you have an existing login, please RESET YOUR PASSWORD before signing in. After you log in for the first time, you will be prompted to confirm your profile preferences, which will be used to personalize content.
We encourage you to explore the new website and visit your updated My RAPS page. If you need assistance, please review our FAQ page.
We welcome your feedback. Please let us know how we can continue to improve your experience.