Symbol | Reference Source | Title | Description |
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ISO 15223-1:20215.4.2 | Do not re-use | Indicates a medical device that is intended for one single use only |
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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 |
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ISO 15223-1:20215.2.3 | Sterilized using ethylene oxide | Indicates a medical device that has been sterilized using ethylene oxide |
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ISO 15223-1:20215.3.2 | Keep away from sunlight | Indicates a medical device that needs protection from light sources |
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ISO 15223-1:20215.3.4 | Keep dry | Indicates a medical device that needs to be protected from moisture |
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Originates from symbol ISO 15223-1:20215.4.5 but crossed out. | Not made with natural rubber latex | |
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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. |
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ISO 15223-1:20215.2.11 | Single sterile barrier system | Indicates a single sterile barrier system |
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MDR Annex V
2017/745 |
CE-mark with Notified Body identification number 2862 | |
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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. |
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ISO 15223-1:20215.1.1 | Manufacturer | Indicates the medical device manufacturer |
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ISO 15223-1:20215.7.7 | Medical device | Indicates the item is a medical device |
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ISO 15223-1:20215.4.3 | Consult instructions for use. | Indicates the need for the user to consult the instructions for use |
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ISO 15223-1:20215.2.6 | Do not resterilize | Indicates a medical device that is not to be resterilized |
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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 |
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ISO 15223-1:20215.1.5 | Batch code | Indicates the manufacturer’s batch code so that the batch or lot can be identified |
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ISO 15223-1:20215.1.4 | Use-by date | Indicates the date after which the medical device is not to be used |
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ISO 15223-1:20215.1.3 | Date of manufacture | Indicates the date when the medical device was manufactured |
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ISO 15223-1:20215.7.10 | Unique Device Identifier. | Indicates a carrier that contains unique device identifier information |
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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. |