TS EN 980

TS EN 980 defines symbols used in the labelling of medical devices and in the information supplied by the manufacturer with those devices. It brings together the graphical language used to replace or supplement words on medical device information so that the meaning can be communicated consistently across markets.

The role of symbols in medical device labelling

In the medical device field, symbols help convey instructions for use, storage conditions, sterility status, batch or lot identification, manufacturer details, and related information in a concise, language-independent form. In general technical terms, this improves consistency across different markets and keeps labels clearer and easier to navigate. The meaning of a symbol, however, should rest on an established standard rather than on informal familiarity, which is why symbol systems matter so much in medical products.

What this standard covers

The focus of this document is the symbols used in information supplied by the manufacturer together with medical devices. In other words, it addresses the shared notation used to present device information, not the device’s clinical performance or the way it is used in practice. Because medical labelling supports safe use, traceability, and correct product identification, symbol standardisation is an important part of the information chain.

• Graphical symbols that support or replace written wording
• Signs used in information supplied by the manufacturer with the device
• A common technical meaning for medical device labelling and information presentation

From a broader technical perspective, a symbol standard like this helps users recognise the same information more easily across languages. The key value of TS EN 980 is its focus on a common symbol approach for medical labelling; detailed product information management is handled together with other related medical device information standards.