Check out our comprehensive glossary of technical symbols for a clear and quick understanding.

Glossary of symbols

Quickly find the medical symbol you need
Reference: 21 CFR 801.15(c)(1)(i) F21 CFR 801.109
Source: Code of Federal Regulations Title 21

For use only on prescription

Warning: According to federal law American, this device cannot be sold only by a doctor or on medical prescription.
Reference: Annex V
Source: European Medical Devices Regulation 2017/745

CE marking

Means technical compliance European.
Source: GOV.UK

UK CA Brand

Means technical compliance of the competent authority of the United Kingdom.
Source: SWISSMEDIC.CH

Agent established in Switzerland

Indicates the contact details of the agent established in Switzerland.
Reference: 5.1.1
Source: EN ISO 15223-1:2021

Manufacturer

Indicates the manufacturer of the medical device.
Reference: 5.1.2
Source: EN ISO 15223-1:2021

Representative established in the European Community

Indicates the agent established in the European Community.
Reference: 5.1.3
Source: EN ISO 15223-1:2021

Date of manufacture

Indicates the date of manufacture of the medical device.
Reference: 5.1.4
Source: EN ISO 15223-1:2021

Expiration date

Indicates the expiry date of the medical device.
Reference: 5.1.5
Source: EN ISO 15223-1:2021

Batch code

Indicates the manufacturer's batch code that allows the batch to be identified.
Reference: 5.1.6
Source: EN ISO 15223-1:2021

Catalog reference

Indicates the manufacturer's catalog reference which allows the device to be identified medical.
Reference: 5.1.7
Source: EN ISO 15223-1:2021

Serial number

Indicates the manufacturer's serial number that allows to identify a medical device specific.
Reference: 5.2.1
Source: EN ISO 15223-1:2021

Sterile

Indicates a medical device that has been subjected to a sterilization process.
Reference: 5.2.2
Source: EN ISO 15223-1:2021

Sterilized using aseptic processing techniques

Indicates a medical device that has been manufactured using techniques recognized aseptics.
Reference: 5.2.3
Source: EN ISO 15223-1:2021

Sterilized with ethylene oxide

Indicates a medical device that has been sterilized with ethylene oxide.
Reference: 5.2.4
Source: EN ISO 15223-1:2021

Sterilized by irradiation

Indicates a medical device that has been sterilized by irradiation.
Reference: 5.2.6
Source: EN ISO 15223-1:2021

Do not resterilize

Indicates a medical device that should not not be resterilized.
Reference: 5.2.7
Source: EN ISO 15223-1:2021

Non-sterile

Indicates a medical device that does not have been subjected to a sterilization process.
Reference: 5.2.8
Source: EN ISO 15223-1:2021

Do not use if packaging is damaged.

Indicates a medical device that should not not be used if the packaging has been damaged or opened.
Reference: 5.3.4
Source: EN ISO 15223-1:2021

Store in a dry place

Indicates a medical device that must be protected from humidity
Reference: 5.3.5
Source: EN ISO 15223-1:2021

Lower temperature limit

Indicates the lower limit of the temperature at which the medical device can be safely exposed.
Reference: 5.3.6
Source: EN ISO 15223-1:2021

Upper temperature limit

Indicates the upper limit of the temperature at which the medical device can be safely exposed.
Reference: 5.3.7
Source: EN ISO 15223-1:2021

Temperature limit

Indicates temperature limits to which the medical device can be safely exposed.
Reference: 5.4.2
Source: EN ISO 15223-1:2021

Do not reuse

Indicates a medical device for use unique or intended for use on a single patient during a single procedure.
Reference: 5.4.3
Source: EN ISO 15223-1:2021

Consult the instructions for use

Indicates the need for the user to consult the instructions for use.
Reference: 5.4.4
Source: EN ISO 15223-1:2021

Warning

Indicates that the user should consult the instructions for obtaining important information such as warnings and precautions that do not may, for various reasons, appear on the medical device.
Reference: 5.6.3
Source: EN ISO 15223-1:2021

Non-pyrogenic

Indicates that the medical device is non-pyrogenic.
Reference: Table D.2, Symbol 10
Source: EN 60601-1:2006

Consult the instruction manual/booklet

Follow the instructions for use.
Reference: Table D.1, Symbol 4
Source: EN 60601-1:2006

Direct current

The electrical medical device is powered by direct current.
Reference: Table D.1, Symbol 9
Source: EN 60601-1:2006

Class II equipment

The electromedical device contains Class II equipment.
Reference: Section 7.4, Figure 9
Source: IEC 60825-1:2014

Laser radiation

The warning label serves as a hazard symbol indicating that the device emits laser light.
Reference: Section 7.4, Figure 9
Source: IEC 60825-1:2014

Do not expose users to telescopic optical components

Warning label indicating that the Laser radiation can be harmful if exposed amplified by optical components telescopic.
Reference: Section 7.4, Figure 9
Source: IEC 60825-1:2014

Do not stare at the beam

Warning label indicating that it Do not look into the laser beam.
Reference: Table 1, Figure 5.7.7
Source: EN ISO 15223-1:2021

Medical device

Indicates that this is a medical device.
Reference: Table 1, Figure 7.3.1
Source: ASTM 2503-20:2020

MRI safe

An item that poses no risk known in all environments magnetic resonance imaging.
Reference: Table 1, Figure 7.3.2.2
Source: ASTM 2503-20:2020

Compatible with MRI under certain conditions

An article that has been shown not to presents no known hazard in a given MRI environment and in conditions of use given.
Reference: Table 23.3 (a), Figure 5.2.11
Source: EN ISO 15223-1:2021

Unique sterile barrier system

Indicates a sterile barrier system unique.
Reference: Table 23.3 (a), Figure 5.2.12
Source: EN ISO 15223-1:2021

Double sterile barrier system

Indicates two sterile barrier systems.
Reference: Table 23.3 (a), Figure 5.2.13
Source: EN ISO 15223-1:2021

Unique sterile barrier system with protective packaging inside.

Indicates a sterile barrier system unique with protective packaging inside.
Reference: Table 23.3 (a), Figure 5.2.14
Source: EN ISO 15223-1:2021

Unique sterile barrier system with protective outer packaging

Indicates a sterile barrier system unique with protective packaging outside.