Major Characteristics for Medical Power Supply
Medical environments are known for its omnipresent risk for both vulnerable and healthy people. To ensure the utmost safety, the design of Medical Power Supplies is monitored by the strictest quality exigences and safety regulations.
As the heart of any electrical medical device, the medical power supplies must comply with the highest standards of performance, safety (IEC 60601) and reliability. Criteria such as MOPP, MOOP, low leakage current, EMC must be taken into consideration during the development stage.
As a result, Medical Power Supplies are equipped with higher levels of insulation and superior EMC performance, and we can distinguish one medically approved Power Supply from other electronics components by its exigent protection level, its high reliability and its extended life cycle of components.
MEAN WELL Medical Power Supplies
MEAN WELL is the global leading manufacturer of Standard Power Supplies in the market. With over 40 years of experience in the development and production of power supplies, MEAN WELL offers the widest range of high-quality Medical Power Supplies in 6 categories as below.
How to choose your Medical Power Supply?
As the keystone of one medical system, it is extremely important to select a safe and reliable Medical Power Supply. To choose the most suitable Medical Power Supply for the Medical system, the R&D engineers are strongly suggested to take, as guideline of selection, the listed criteria below into consideration
A. Electrical requirements
The input voltage range and required power should be defined for the application, as well as its output voltage and the needed current to power the application:
- Input voltage range: the most common input source is an AC source, and the range requirement is related to the destined market of the end devices. In the case of multiple market regions of the Medical system, it is strongly recommended to choose a Medical Power Supply with input voltage range covering at least the range of 100VAC to 240VAC.
- Power requirement: the required power depends mainly on the end device. It is suggested to keep in mind the derating caused by the unfavorable working temperature, as well as the potential peak current.
Output voltage and current: according to the design of the Medical system, some systems demand a constant current output while others need constant voltage. The R&D engineers should choose an adequate Medical Power Supply, with the right level and type of DC output, based on the design of the application.
B. Regulations
As each market territory and each application field imposes its own safety regulations on the end devices, it is crucial to understand which certifications are mandatory for the application and its target market(s) during the development process.
For instance, home healthcare devices are required to meet the standards of IEC 60601-1-11, while for equipment not directly in contact with the patient, IEC 62368 might still give one the possibility to get a medical certification for medical test and measurement equipment on a system level.
Meanwhile, each country adopts its specific safety standards for the application field (e.g. UL ANSI/AAMI ES60601-1 for the US, EN 60601-1 for EU countries, CAN/CSA-C22 3rd edition for Canada…etc.
C. Installation Method
The installation of the PSU can be either internally or externally depending on how the Power Supply is designed to be integrated into the system.
External solution:
Internal solution:
- Medical Enclosed type: PSU with plastic or metal case.
- Medical PCB type: A PCB populated with components which from the power supply. Normally this solution is without any mechanical protection such as a housing. For this reason, normally installed inside an application and not touchable by the user.
- Medical On board or Medical PCB mount: PSU designed to fit on a PCB. It can be either “open frame” or “encapsulated”. The second type is potted with compound to provide protection against external elements (e.g. moisture, corrosive elements, shock, vibration…etc.).
D. Other requirements
Medical systems are regulated with extremely vigorous exigences. On top of the above criteria, it is also important to verify that the other specific requirements are met:
- Class: Class I or class II
- Heat dissipation: Forced air cooling (with fan) or Passive cooling (without fan)
- Level of protection required: 2 x MOOP, 2 x MOPP
- Leakage current
- Overload protection: Constant Current Limiting or Hiccup mode
- Remote on/off function
- Current sharing function
- Parallel function
- …
Specific Requirements for Medical Power Supplies
I. IEC 60601-1:
Defined by the world known International Electrotechnical Commission (IEC), IEC 60601-1 is a series of technical standards destined to ensure the safety and performance of electrical equipment in the medical industry. On one hand, some digression from the IEC 60601-1 standards exists. For example, EN 60601-1 for Europe and ES 60601-1 for the US market which are harmonized with the IEC standards. One the other hand, there are also some “collateral” standards to IEC 60601-1; such as IEC 60601-1-2 which is the 4th edition of collateral EMC standards to IEC 60601-1.
II. MOOP and MOPP
In the medical environment, risk is constantly present for patient and/or operator of a medical device. Aiming to protect both groups from electrical medical devices, MOOP and MOPP are introduced to monitor the level of insulation.
- MOOP stands for Means of Operator Protection. This category is related to electronic devices which are handled by trained operators, and do not come into direct contact with the patient. The medical device with 2 x MOOP has an isolation of 3000V AC isolation.
- MOPP, on the other hand, is the Means of Patient Protection; all electronic devices with direct physical contact with patients must meet stricter standards and require a double isolation between input and output.
Presuming that patients are vulnerable; MOPP standards are specially designed to protect them from any potential electric shock. In the design, MOPP requires the medical devices to have two separate insulation barriers.
Therefore, devices are MOOP and MOPP classified depending on the type of contact with patients and operators.
Classification | Required Isolation | Required Creepage | Requirement Insulation |
MOOP | 1500V AC | 2.5mm | – |
2 x MOOP | 3000V AC | 5mm | Reinforced |
MOPP | 1500V AC | 5mm | – |
2 x MOPP | 4000V AC | 8mm | Reinforced |
1 MOOP and MOPP under IEC60601-1 are different in the levels of isolation, creepage, insulation.
III. Low leakage current
The essential use of medical equipment is on the human body, therefore the chance and duration of contact with this equipment is higher and longer. Having electric current running throughout the body can be extremely dangerous and might even result in death. For example, a current as low as 40mA could already be fatal to a healthy person, while a weakened person’s tolerance is even lower.
To protect all people in contact with the devices from the electric shock, medical power supplies must meet strict requirements in terms of leakage current. While Applied Parts (AP) indicate the parts of a Medical device or a Medical system which, during normal use, come into direct physical contact with a patient. The standards of IEC60601-1 give a clear definition of the acceptable values of leakage current for each classification of Applied Parts (AP), and the classifications are further divided into 2 categories: “NC” for normal condition and “SFC” for Single fault condition.
Leakage Current |
Type B | Type BF | Type CF | |||
NC | SFC | NC | SFC | NC | SFC | |
Earth Leakage Current | 5mA | 10mA | 5mA | 10mA | 5mA | 10mA |
Enclosure Leakage Current | 100µA | 500µA | 100µA | 500µA | 100µA | 500µA |
Patient Leakage Current | 100µA | 500µA | 100µA | 500µA | 10µA | 50µA |
2 Different Leakage Current limits defined by IEC60601-1 according to the medical environment: Type B, Type BF, Type CF
IV. Classification of medical environment
Just like medical power supplies, end systems in medical environments are also regulated by strict isolation and leakage current requirements.
Depending on the type of physical contact between patient and medical device, there are three main classification types of Applied Parts (AP) in the medical environment: Type B, Type BF, Type CF.
- Type B (Body)
Devices with no direct physical contact with patients. Examples: medical bed, medical laser…etc. - Type BF (Body Float)
Devices with physical contact with patients and might present risk in the case of device failure. Examples: Incubators, diagnostic equipment, etc. - Type CF (Cardiac Float)
Direct contact to the patient’s heart, risk of injury or death in the event of device failure. Examples: Defibrillators, heart-lung machines, etc.
Note: Medical power supplies for type BF & CF devices are designed to meet 2 x MOPP
V. EMC standard and limits
Malfunction induced by electromagnetic or interference could be fatal when it comes to life-saving devices. The EMC standards EN 55011 for electromagnetic interference and IEC 60601-1-2 with reference and electromagnetic immunity must be considered.
The 4th edition of the IEC-60601-1 standard on EMC is much more vigorous with electromagnetic immunity than the previous edition. Medical devices must now be immune to HF fields up to 2.7GHz, which represent an increase by 0.2GHz. To prevent damage caused by electrostatic discharge, the limits have also been increased accordingly. For contact discharge, the level has been increased from 6 to 8kV. For air discharge, it has been increased from 8 to 15kV compared to the previous edition.
VI. EU Medical Device regulation (MDR)
The European Union Medical Device Regulation (MDR) published 2017, will soon replace the current Medical Device Directive (MDD) (93/42/EEC) and the EU’s Directive on active implantable medical devices (90/385/EEC). All development engineers and manufacturers related to Medical Devices within Europe will need to follow the Medical Device Regulation of 2017 published by European Parliament.
VII. ISO 13485
ISO 13485 is the standard for the quality management system for medical devices. The requirements are destined to organizations involved in the design, production, storage, installation and maintenance of medical devices and other related services.
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