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ISO 15223-1 / Medical devices-Symbols to be used with medical device labels, labelling and Informationen to be supplied |
5.1.1 / Manufacturer |
Indicates the medical device manufacturer |
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ISO 15223-1 / Medical devices-Symbols to be used with medical device labels, labelling and Informationen to be supplied |
5.1.2 / Authorized representative in the European Community |
Indicates the authorized representative in the European union. Symbol is accompanied by the Name and address of the authorized representative adjacent to the symbol |
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ISO 15223-1 / Medical devices-Symbols to be used with medical device labels, labelling and Informationen to be supplied |
5.1.3 / Date of Manufacture |
Indicates the date when the medical device was manufactured |
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ISO 15223-1 / Medical devices-Symbols to be used with medical device labels, labelling and Informationen to be supplied |
5.1.4 / Use-by-date |
Indicates the date after which the medical device is not to be used |
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ISO 15223-1 / Medical devices-Symbols to be used with medical device labels, labelling and Informationen to be supplied |
5.1.5 / Batch code |
Indicates the manufacturer's batch code or lot can be identified |
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ISO 15223-1 / Medical devices-Symbols to be used with medical device labels, labelling and Informationen to be supplied |
5.1.6 / Catalogue number |
Indicates the manufacturer's catalogue number so the medical device can be identified |
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ISO 15223-1 / Medical devices-Symbols to be used with medical device labels, labelling and Informationen to be supplied |
5.1.7 / Serial number |
Indicates the manufacturer's serial number so that a specific medical device can be identified |
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ISO 15223-1 / Medical devices-Symbols to be used with medical device labels, labelling and Informationen to be supplied |
5.2.8 / Do not use if package is damaged |
Indicates a medical device that should not be used if the package has been damaged or opened |
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ISO 15223-1 / Medical devices-Symbols to be used with medical device labels, labelling and Informationen to be supplied |
5.3.1 / Fragile, handle with Versorgung |
Indicates a medical device that can be broken or damaged if not handled carefully |
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ISO 15223-1 / Medical devices-Symbols to be used with medical device labels, labelling and Informationen to be supplied |
5.3.4 / Keep dry |
Indicates a medical device that needs to be protected from moisture |
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ISO 15223-1 / Medical devices-Symbols to be used with medical device labels, labelling and Informationen to be supplied |
5.3.5 / Lower limit of temperature |
Indicates the lower limit of temperature to which the medical device can be safely exposed |
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ISO 15223-1 / Medical devices-Symbols to be used with medical device labels, labelling and Informationen to be supplied |
5.3.6 / Upper limit of temperature |
Indicates the upper limit of temperature to which the medical device can be safely exposed |
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ISO 15223-1 / Medical devices-Symbols to be used with medical device labels, labelling and Informationen to be supplied |
5.3.7 / Temperature limit |
Indicates the temperature limits to which the medial device can be safely exposed |
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ISO 15223-1 / Medical devices-Symbols to be used with medical device labels, labelling and Informationen to be supplied |
5.3.8 / Humidity limitation |
Indicates the Spektrum of humidity to which the medical device can be safely exposed |
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ISO 15223-1 / Medical devices-Symbols to be used with medical device labels, labelling and Informationen to be supplied |
5.3.9 / Atmospheric pressure limitation |
Indicates the Spektrum of atmospheric pressure to which the medical device can be safely exposed |
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ISO 15223-1 / Medical devices-Symbols to be used with medical device labels, labelling and Informationen to be supplied |
5.4.3 / Consult instructions for use |
Indicates the need for the user to consult the instructions for use |
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ISO 15223-1 / Medical devices-Symbols to be used with medical device labels, labelling and Informationen to be supplied |
5.4.4 / Caution |
Indicates the need for the user to consult the instructions for use for important Informationen such as warnings and cautions |
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IEC 60417 / Graphical symbols for use on equipment |
5333 / Type BF applied part |
Identifies a type BF applied part complying with IEC 60601-1 |
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IEC 60417 / Graphical symbols for use on equipment |
5840 / Type B applied part |
Identifies a type B applied part complying with IEC 60601-1 |
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IEC 60417 / Graphical symbols for use on equipment |
5172 / Class II equipment |
Identifies equipment meeting the safety requirements specified for Class II equipment according to IEC 61140 |
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IEC 60417 / Graphical symbols for use on equipment |
5926 / Polarity of d. c. power connector |
Identifies the positive and negative connections of a d. c. power supply |
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IEC 60417 / Graphical symbols for use on equipment |
5957 / For indoor use only |
Identifies electrical equipment konzipiert for indoor use |
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IEC 60417 / Graphical symbols for use on equipment |
5032 / Alternating Current |
Indicates that the equipment is geeignet for alternating current only; to identify relevant terminals |
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IEC 60417 / Graphical symbols for use on equipment |
5031 / Direct current |
Indicates that the equipment is geeignet for direct current only; to identify relevant terminals |
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IEC 60417 / Graphical symbols for use on equipment |
5140 / Non-ionizing electromagnetic radiation |
Indicates generally elevated, potentially hazardous, levels of non-ionizing radiation, or to indicate equipment or systems e.g. that intentionally apply RF electromagnetic for diagnosis or Behandlung |
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IEC 60417 / Graphical symbols for use on equipment |
5009 / Stand-by |
Identifies the switch or switch position by means of which part of the equipment is switched on in order to bring it into the standby condition |
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IEC 60417 / Graphical symbols for use on equipment |
5016 / Fuse |
Identifies fuse boxes or their locations |
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IEC 60417 / Graphical symbols for use on equipment |
5008 / “OFF” |
Indicates disconnection from the mains, at least for mains switches or their positions, and all those cases where safety is involved |
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IEC 60417 / Graphical symbols for use on equipment |
5007 / “ON” |
Indicates connection to the mains, at least for mains switches or their positions, and all those cases where safety is involved |
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IEC 60417 / Graphical symbols for use on equipment |
5104 / Start; start of action |
Identifies the start button |
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ISO 7010 / Graphical symbols — Safety colours and safety signs — Registered safety signs |
M002 / Refer to instruction manuell / booklet |
Indicates that the instruction manuell / booklet must be read |
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ISO 7010 / Graphical symbols — Safety colours and safety signs — Registered safety signs |
P007 / No access for people with active implanted kardial devices |
Indicates that people with active implanted kardial devices are prohibited from entering a designated area |
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ISO 7000 / Graphical symbols for use on equipment |
0623 / This way up |
Indicates the correct upright position of a package |
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IEC 60529 / Degrees of protection provided by enclosures (IP Code) |
N/A |
Protected against solid objects over 12.5mm (e.g., a finger) and no protection against liquids |
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IEC 60529 / Degrees of protection provided by enclosures (IP Code) |
N/A |
Protected against solid objects over 12.5mm (e.g., a finger) and protected against vertically falling drops of water or condensation |
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IEC 60529 / Degrees of protection provided by enclosures (IP Code) |
N/A |
Protected against solid objects over 12.5mm (e.g., a finger) and protected against falling drops of water, if the case is disposed at any angle up to 15 degrees from vertical |
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IEC 60529 / Degrees of protection provided by enclosures (IP Code) |
No specific reference no. / IP Classification |
Protected from limited dust ingress. Protected from water spray from any direction, limited ingress protection |
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IEC 60529 / Degrees of protection provided by enclosures (IP Code) |
No specific reference no. / IP Classification |
Protected from limited dust ingress. Protected from water jets from any direction, limited ingress protection |
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21 CFR 801.109 / Prescription Devices |
Prescription Device |
Indicates that the Produkt is a medical device and Federal Law (USA) restricts this device to sale by or on the order of a physician |
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Medical Devices Directive 93/42/EEC |
CE Marking |
CE marking indicates that a Produkt complies with applicable European Union regulations |
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BS EN 50419, Marking of electrical and electronic equipment in accordance with article 11(2) of Directive 2002/96/EC (WEEE) |
Crossed out wheelie bin |
Indicates a Produkt should not be disposed of in a landfill; the black bar indicates that the equipment was manufactured after 2005 |
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Federal Communications Commission |
FCC Marking |
FCC marking indicates the electronic device, which sold in the United States, is certified and the electromagnetic interference from the device is under the limits that are approved by Federal Communications Commission |
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N/A |
Cuff Positioning |
Indicates the correct positioning for the Monitor on the wrist |
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N/A |
Cuff Positioning |
Indicates the correct positioning for the Monitor on the wrist |
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N/A |
Artery Marks |
Types of marks used to indicate the correct positioning of the artery for the upper arm |
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N/A |
Cuff Positioning |
Indicator on the cuff for left upper arm |
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N/A |
Cuff Indicator |
Spektrum pointer and brachial artery alignment positioning indicator on the cuff |
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N/A |
Cuff Identifier |
Identifies the type of cuff that is compatible with the blood pressure Monitor |
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N/A |
Cuff Identifier |
Identifies the type of cuff that is compatible with the blood pressure Monitor |
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N/A |
Arm Circumference Spektrum |
Indicates the Spektrum of arm circumferences to help with selection of the correct cuff size |
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N/A |
Warnings |
Various Warnung symbols to indicate a potentially hazardous situation which, if not avoided, could result in death or serious injury |
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N/A |
Marking for the position of the replaceable air tube |
Indicates the position to insert the air tube |
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