E DIN EN IEC 61340-6-1/A1 VDE 0300-6-1/A1:2024-10

Electrostatics

Part 6-1: Electrostatic control for healthcare – General requirements for facilities

NEW DIN EN IEC 60601-2-19 VDE 0750-2-19:2024-10

Medical electrical equipment

Part 2-19: Particular requirements for the basic safety and essential performance of infant incubators

NEW DIN EN IEC 60601-2-20 VDE 0750-2-20:2024-10

Medical electrical equipment

Part 2-20: Particular requirements for the basic safety and essential performance of infant transport incubators

NEW DIN EN IEC 60601-2-21 VDE 0750-2-21:2024-10

Medical electrical equipment

Part 2-21: Particular requirements for the basic safety and essential performance of infant radiant warmers

DIN EN IEC 60601-2-50 VDE 0750-2-50:2024-09

Medical electrical equipment

Part 2-50: Particular requirements for the basic safety and essential performance of infant phototherapy equipment

DIN EN IEC 60601-2-76 VDE 0750-2-76:2024-09

Medical electrical equipment

Part 2-76: Particular requirements for the basic safety and essential performance of low energy ionized gas haemostasis equipment

DIN EN IEC 80601-2-77 VDE 0750-2-77:2024-09

Medical electrical equipment

Part 2-77: Particular requirements for the basic safety and essential performance of robotically assisted surgical equipment

E DIN EN IEC 80601-2-71 VDE 0750-2-71:2024-08

Medical electrical equipment

Part 2-71: Particular requirements for the basic safety and essential performance of functional near-infrared spectroscopy (NIRS) equipment

DIN EN IEC 60601-2-43 VDE 0750-2-43 Berichtigung 1:2024-07

Medical electrical equipment

Part 2-43: Particular requirements for the basic safety and essential performance of X-ray equipment for interventional procedures

DIN VDE V 0750-2-52-2 VDE V 0750-2-52-2:2024-05

Medical electrical equipment

Part 2-52-2: Particular requirements for basic safety and essential performance of couches

DIN EN IEC 80601-2-59 VDE 0750-2-59:2024-03

Medical electrical equipment

Part 2-59: Particular requirements for the basic safety and essential performance of screening thermographs for human febrile temperature screening

An english translation of this document is available.

DIN EN IEC 60601-2-43 VDE 0750-2-43:2024-02

Medical electrical equipment

Part 2-43: Particular requirements for the basic safety and essential performance of X-ray equipment for interventional procedures

An english translation of this document is available.

E DIN EN IEC 60601-2-37 VDE 0750-2-37:2023-12

Medical electrical equipment

Part 2-37: Particular requirements for the basic safety and essential performance of ultrasonic medical diagnostic and monitoring equipment

DIN EN IEC 61689 VDE 0754-3:2023-12

Ultrasonics

Physiotherapy systems – Field specifications and methods of measurement in the frequency range 0,5 MHz to 5 MHz

An english translation of this document is available.

DIN EN 50527-2-3 VDE 0848-527-2-3:2023-12

Procedure for the assessment of the exposure to electromagnetic fields of workers bearing active implantable medical devices

Part 2-3: Specific assessment for workers with implantable neurostimulators;

An english translation of this document is available.

DIN EN ISO 14708-4 VDE 0750-20-4:2023-09

Implants for surgery – Active implantable medical devices

Part 4: Implantable infusion pump systems

DIN IEC/TR 61390 VDE 0754-4:2023-09

Ultrasonics

Real-time pulse-echo systems – Test procedures to determine performance specifications

An english translation of this document is available.

E DIN EN IEC 60601-2-2/A1 VDE 0750-2-2/A1:2023-05

Medical electrical equipment

Part 2-2: Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories

E DIN EN IEC 60601-2-57 VDE 0750-2-57:2023-03

Medical electrical equipment

Part 2-57: Particular requirements for the basic safety and essential performance of non-laser light source equipment intended for therapeutic, diagnostic, monitoring and cosmetic/aesthetic use

DIN EN IEC 80001-1 VDE 0756-1:2023-02

Application of risk management for IT-networks incorporating medical devices

Part 1: Safety, effectiveness and security in the implementation and use of connected medical devices or connected health software

An english translation of this document is available.