Symbol Reference Source Title Description
ISO 15223-1:20215.4.2 Do not re-use Indicates a medical device that is intended for one single use only
ISO 15223-1:20215.2.8 Do not use if package is damaged and consult instructions for use Indicates that a medical device that should not be used if the package has been damaged or opened and that the user should consult the instructions for use for additional information
ISO 15223-1:20215.2.3 Sterilized using ethylene oxide Indicates a medical device that has been sterilized using ethylene oxide
ISO 15223-1:20215.3.2 Keep away from sunlight Indicates a medical device that needs protection from light sources
ISO 15223-1:20215.3.4 Keep dry Indicates a medical device that needs to be protected from moisture
Originates from symbol ISO 15223-1:20215.4.5 but crossed out. Not made with natural rubber latex
ISO 60601-1
IEC 60417-5335
Annex D, table D1
Not defibrillation-proof Warning: This device is not defibrillation-proof
and should not be used with defibrillation-proof ECG connections.
ISO 15223-1:20215.2.11 Single sterile barrier system Indicates a single sterile barrier system
MDR Annex V

2017/745

CE-mark with Notified Body identification number 2862
ISO 15223-1:20215.1.6 Catalogue number Indicates the manufacturer’s catalogue number so that the medical device can be identified
Rx only 21 CFR 801.109 Prescription devices Caution: Federal (US) law restricts this device to sale by or on the order of a physician.
ISO 15223-1:20215.1.1 Manufacturer Indicates the medical device manufacturer
ISO 15223-1:20215.7.7 Medical device Indicates the item is a medical device
ISO 15223-1:20215.4.3 Consult instructions for use. Indicates the need for the user to consult the instructions for use
ISO 15223-1:20215.2.6 Do not resterilize Indicates a medical device that is not to be resterilized
ISO 15223-1:20215.4.4 Caution Indicates that caution is necessary when operating the device or control close to where the symbol is placed, or that the current situation needs operator awareness or operator action in order to avoid undesirable consequences
ISO 15223-1:20215.1.5 Batch code Indicates the manufacturer’s batch code so that the batch or lot can be identified
ISO 15223-1:20215.1.4 Use-by date Indicates the date after which the medical device is not to be used
ISO 15223-1:20215.1.3 Date of manufacture Indicates the date when the medical device was manufactured
ISO 15223-1:20215.7.10 Unique Device Identifier. Indicates a carrier that contains unique device identifier information
WEEE directive 2012/19/EU Recycle: Electronic Equipment Indicates that the product should not be discarded as unsorted waste but must be sent to separate collection facilities for recovery and recycling.

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