ISO 15223-1:2020 new symbols for medical devices
In this paragraph, we will talk about the update of ISO 15223-1 that will introduce new symbols to add in the labelling of medical devices. Specifically, along with ISO 20471, the new ISO 15223 is a fundamental standard to support the manufacturers in preparation of labelling and accompanying documents. For instance, after the new regulation on risk management, this is an important update for medical device industry.
New Symbols for ISO 15223-1:2020
Firstly, these are the general new symbols:
- Symbols if the device is a Medical Device (MD) or In-Vitro Diagnostic (IVD).
Moreover, for the IVD symbol, it is important to mention that the symbols is to identify in-vitro diagnostic devices and not medical devices to be used in vitro.
- Symbols to identify the repackaging of a device.
This symbol means that a modification of the original medical device packaging has been performed. The name and address of the responsible for repackaging activity shall be mentioned adjacent to the symbol. This symbols is used only when the repackaging is not performed by the manufacturer.
- UDI symbol.
The UDI symbols is optional. When multiple data carrier are present on the label, the symbol may be used.
- Name of the patient (for particular medical device).
The symbol indicates the name of the patient
- Symbols to inform that some information for use are available on the web.
This symbol indicates that a patient can obtain additional information on the medical product. This symbol shall be accompanied by the web address adjacent to the symbol.
New Symbols related to Economic Operators
Furthermore, there are two symbols to identify economic operators under EU MDR and IVDR:
Importantly, this symbol indicates the entity importing the medical device into the locale. This symbol is accompanied by the name and address of the importing entity, adjacent to the symbol.
For instance, the EU MDR 2017/745 specifies in details the role of these two economic operators within European Union.
New Symbols for sterile medical devices
Moreover, there are new indications to identify the type of sterile barriers for sterile medical devices:
- Singe Sterile Barrier System
The symbol indicates a single sterile barrier system.
- Double Sterile Barrier System it is a very similar to the previous symbol, but it contains two lines and not one.
- Singe Sterile Barrier System with protective packaging inside
Specifically, this symbol indicates a single sterile barrier system with protective packaging inside. The protective packaging located inside the sterile barrier system prevents damage to the contents or to help with aseptic presentation. It does not provide a microbial barrier to maintain sterility.
- Singe Sterile Barrier System with protective packaging outside. This is a very similar symbol respect the previous one, but the dotted line is external to the continuous line. The protective packaging outside the sterile barrier system prevents damage to the sterile barrier system and the contents. The protection is against physical hazards, particulate contamination or other environmental hazards, but it does not include a microbial barrier.
Furthermore, there are as well new symbols to warn the user about biohazard-related risks.
Specifically, there are new symbols for medical devices containing:
- human blood or plasma derivatives;
This symbol indicates a medical device that contains or incorporates human blood or plasma derivatives.
- a medicinal substances;
This symbol indicates a medical device that contains or incorporates a medicinal substance.
- biological material of animal origin;
The symbol indicates a medical device that contains biological tissue, cells, or their derivatives, of animal origin.
- biological material of human origin.
This symbol indicates a medical device that contains biological tissue, cells, or their derivatives, of human origin
This is just a high level overview of the new symbols for labelling of medical devices introduced with the update of ISO 15223-1.
Specifically, the publication of the revised standard will occur in Q4 2020, along with ISO 20471 that will deal with information to be provided by medical device manufacturers.
To conclude, this is in the contest of waiting some future updates for ISO 13485 which could take big advantage from this new specific ISO standard. Furthermore, for an overview of ISO 13485 requirements, see this post on QualityMedDev. Do not forget to have a look to our WhitePaper on Biocompatibility Evaluation for Medical Devices.