Standard:
PREORDER DIN VDE V 0100-710-1 VDE V 0100-710-1:2025-10Medical locations Part 710-1: Requirements of the expected HD 60364-7-710 |
Draft:
PREORDER E DIN EN ISO 80601-2-13/A1 VDE 0750-2-13/A1:2025-10Medical electrical equipment Part 2-13: Particular requirements for basic safety and essential performance of an anaesthetic workstation |
Standard:
PREORDER DIN EN IEC 60601-2-39 VDE 0750-2-39:2025-10Medical electrical equipment Part 2-39: Particular requirements for the basic safety and essential performance of peritoneal dialysis equipment |
Draft:
PREORDER E DIN EN IEC 80601-2-60/A1 VDE 0750-2-60/A1:2025-10Medical electrical equipment Part 2-60: Particular requirements for the basic safety and essential performance of dental equipment |
Standard:
PREORDER DIN IEC 63310 VDE 0750-34-5:2025-10Functional performance criteria for AAL robots used in connected home environment
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Draft:
NEW E DIN EN IEC 80601-2-31 VDE 0750-2-31:2025-09Medical electrical equipment Part 2-31: Particular requirements for the basic safety and essential performance of external cardiac pacemakers with internal power source |
Standard:
DIN EN IEC 60601-2-34 VDE 0750-2-34:2025-08Medical electrical equipment Part 2-34: Particular requirements for the basic safety and essential performance of invasive blood pressure monitoring equipment An english translation of this document is available. |
Standard:
DIN EN 60601-1 VDE 0750-1 Berichtigung 1:2025-07Medical electrical equipment Part 1: General requirements for basic safety and essential performance |
Standard:
DIN EN 60601-2-3 VDE 0750-2-3:2025-07Medical electrical equipment Part 2-3: Particular requirements for the basic safety and essential performance of short-wave therapy equipment |
Standard:
DIN EN 60601-2-6 VDE 0750-2-6:2025-07Medical electrical equipment Part 2-6: Particular requirements for the basic safety and essential performance of microwave therapy equipment |
Standard:
DIN EN IEC 60601-2-21 VDE 0750-2-21 Berichtigung 1:2025-07Medical electrical equipment Part 2-21: Particular requirements for the basic safety and essential performance of infant radiant warmers |
Standard:
DIN EN IEC 60601-2-33 VDE 0750-2-33:2025-07Medical electrical equipment Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis An english translation of this document is available. |
Draft:
E DIN EN IEC 61326-2-6 VDE 0843-20-2-6:2025-07Electrical equipment for measurement, control and laboratory use – EMC requirements Part 2-6: Particular requirements – In vitro diagnostic (IVD) medical equipment |
Standard:
DIN EN IEC 60601-2-2 VDE 0750-2-2:2025-06Medical electrical equipment Part 2-2: Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories An english translation of this document is available. |
Draft:
E DIN EN IEC 80601-2-23 VDE 0750-2-23:2025-06Medical electrical equipment Part 2-23: Particular requirements for the basic safety and essential performance of transcutaneous partial pressure monitoring equipment |
Standard:
DIN EN IEC 60601-2-37 VDE 0750-2-37:2025-06Medical electrical equipment Part 2-37: Particular requirements for the basic safety and essential performance of ultrasonic medical diagnostic and monitoring equipment An english translation of this document is available. |
Standard:
DIN EN IEC 80601-2-49 VDE 0750-2-49:2025-06Medical electrical equipment Part 2-49: Particular requirements for the basic safety and essential performance of multifunction patient monitoring equipment An english translation of this document is available. |
Standard:
DIN EN ISO 20342-1 VDE 0750-2-52-1:2025-06Assistive products for tissue integrity when lying down Part 1: General requirements |
Standard:
DIN IEC/TS 60601-4-2 VDE V 0750-4-2:2025-06Medical electrical equipment Part 4-2: Guidance and interpretation – Electromagnetic immunity: performance of medical electrical equipment and medical electrical systems An english translation of this document is available. |
Standard:
DIN IEC 63240-1 VDE 0754-5-1:2025-06Active assisted living (AAL) reference architecture and architecture model Part 1: Reference architecture An english translation of this document is available. |