Naturally, multiple socket-outlets are needed for medical devices in daily practice as well. However, a lot of people are unaware of the regulatory consequences of using multiple socket-outlets.
This article will give you the necessary overview:
Operators, e.g. hospitals, use multiple socket-outlets to:
IEC 60601-1 defines the term multiple socket-outlet as follows:
“one or more socket-outlets intended to be connected to, or integral with, flexible cables or cords or ME EQUIPMENT for SUPPLY MAINS or equivalent voltage”
Source: IEC 60601-1
Multiple socket-outlets are often used on equipment trolleys in hospitals, e.g., for endoscopies, rounds or ultrasound equipment. In these cases, you come across multiple socket-outlets:
IEC 60601-1 has good reasons to specifically regulate the use of multiple socket-outlets:
A common protective earth conductor: A multiple socket-outlet has one common protective earth conductor (PE conductor) for all connected devices. In other words, if the protective earthing fails, it fails for all the devices.
In this example, the total impedance of the protective earthing system is calculated from the sum of the impedances of the building protective earth, the multiple socket-outlet, the power supply cord and the device-internal protective earth system - 0.5 ? in the example.
Even if each part meets the requirements individually, a short circuit (earth contact) in the ME equipment would lead to an excessively high touch voltage and thus to a high touch current. In the worst case, the impedance of the protective earth system can limit the short-circuit current to such an extent then the fuse is not tripped.
These two cases must be avoided under all circumstances.
Fig. 1: Risk of an electrical hazard in the event of a short circuit (earth contact) and increased PE resistance. The multiple socket-outlet contributes to the overall impedance.
If several ME devices and non-ME devices are connected via one multiple socket-outlet, the earth leakage currents (IEL1, IEL2, IEL3) of all devices in the protective earth system of the multiple socket are added together. In the event of a single fault condition in the multiple socket-outlet, there may be an increased touch current It. In addition, an interruption in the mains conductor of the multiple socket-outlet can lead to all the ME equipment cutting out.
Fig. 2: The earth leakage current I-total must not exceed 5 mA in the normal state or 10 mA in a single fault condition.
All in all, the following hazards (among others) are generated:
However, we should also mention a positive side effect: A multiple socket-outlet acts a potential equalizer for the connected devices.
In the general safety and performance requirements, the EU directives (e.g., MDD) and EU regulations (e.g., MDR) explicitly require electrical, thermal and functional safety, i.e., the protection of patients and users from the aforementioned hazards.
National laws make these requirements their own and add to them, for example with national regulations such as the German MPBetreibV [Medical Devices Operator Ordinance].
In order to demonstrate compliance with these requirements, manufacturers should (must) comply with the relevant (harmonized) standards such as IEC 60601-1 and IEC 60884-1 (“Plugs and socket-outlets for household and similar purposes - Part 1: General requirements”).
Because multiple socket-outlets as described above can have a significant effect on the safety of an ME system, the standard also explicitly establishes requirements for multiple socket-outlets and for devices with integrated multiple socket-outlets.
It stipulates that manufacturers (including operators) must assess components for their suitability for the operating conditions. This includes aspects such as:
The standards specifically require:
Section 188.8.131.52 of the standard provides a summary of the most important requirements regarding the use of MSOs in ME systems.
Standard multiple socket-outlets from a hardware store are therefore not suitable for use in a ME system or in rooms used for medical purposes.
The following, for example, are not permitted:
On the other hand, it is permissible for the impedance of the protective earth to exceed the specified values, if the touch current and the patient leakage current are not exceeded in a single fault condition.
Manufacturers who use a multiple socket-outlet in an ME system or ME equipment are responsible for it. Operators who (mostly unknowingly) build an ME system must also accept this responsibility as soon as equipment is connected via an MSO. An organization then automatically becomes the manufacturer, assumes responsibility and must, therefore, comply with the requirements of the standard.
For ME systems marketed by the manufacturer, only devices intended for the ME system may be connected to multiple socket-outlets. A multiple socket-outlet must be clearly marked to show the devices that may be connected according to the intended purpose.
The manufacturer must describe how to use the multiple outlet-socket in the instructions for use and give a warning stating that no additional MSOs may be connected and that the MSO must not be placed on the floor. Incidentally, the instructions for use are part of the ME system.
If a non-ME device is part of an ME system for which the manufacturer has provided an isolating transformer, the instructions for use must inform the user that the non-ME device must be plugged into another socket-outlet.
The manufacturer must cover unused open socket-outlets on an MSO in such a way that the covers can only be removed with a tool.
The manufacturer must protect the socket against unintentional unplugging.
Various protective measures are recommended, depending on the specific application.
Fig. 3: Protective measures minimize the risks associated with equipment connected via multiple socket-outlets.
Testing is done:
If the manufacturer markets the ME system as a single item, the manufacturer tests it together with the testing laboratory.
If, on the other hand, the operator builds the ME system, the operator is also responsible for testing. This also applies if the operator adds to a manufacturer’s ME system.
The manufacturer and/or operator should be able to provide the following documentation following these tests:
When do I need an isolating transformer? Where can it be installed?
An isolating transformer is in fact always required if non-ME devices are involved. Table I.1 of the standard gives an overview with various set-ups and recommendations for possible measures.
What alternatives are there to the isolating transformer?
One alternative is, for example, using a second protective earth conductor in a non-ME device. This means that the single fault safety is ensured if the primary protective earth conductor is interrupted.
What leakage currents have be complied out?
In the patient environment: TOUCH CURRENT 500 ?A
Which tests or certifications do I need? Are accredited laboratories necessary?
What components have to be used? Do they have to be certified?
It is always helpful to use already tested components (transformers, cables, plugs, PCs, insulations, etc.). If this is not possible, the requirements of the standard must be met.
What does the operator have to do? How does this relate to the safety engineering control?
The operator must comply with the operator ordinance that requires a metrological control and a safety engineering control to be performed at least once per year for certain medical devices. This also applies to installations and systems, such as ME systems, created by the operator themselves and that they operate.
The protective earthing musted be tested by measurement and inspection and the leakage currents must be checked.
Is a multiple socket-outlet a functional connection?
Definition from the standard: Connection, electrical or otherwise, including those intended to transfer signals, data, power or substances.
A functional connection is not necessarily electrical in nature. For example, a data cable is a functional connection. The manufacturer must take the effect of the shield into account. Excess leakage currents can flow via the shield. See figure 3 below.
What is the difference between a system and a procedure pack?
ME system is defined in the standard. If the manufacturer markets a system as a single item, then it may be a procedure pack. However, this is not the same as what the MDR means by the term procedure pack. The standard is about safety and performance.
A procedure pack is defined in Article 12 of the MDD and has a legally defined meaning with regard to conformity with the essential requirements and the operator's responsibilities.
The term is not defined. Helpful definitions:
What is considered in-house production?
If the operator extends the system by connecting devices other than those permitted by the manufacturer or by connecting several ME devices via a multiple socket-outlet for one of the purposes specified in #1.