Our product packaging uses a number of symbols to inform quickly and clearly about contents and use. They conform with the Swedish Standard (SS-EN 980) and the European Standard (EN 908:2008) for the marking of medical devices.
Used symbols – and their meanings:
  • Ateranvand_ej

    Product’s Article no.

  • Ateranvand_ej

    Do not reuse. Use only once.

  • Ateranvand_ej

    Use by. Do not use after the end of the year/month stated.

  • Ateranvand_ej

    Batch code. The code states the producer’s manufacturing code.

  • Ateranvand_ej

    Contains or presence of natural rubber latex

  • Ateranvand_ej

    Manufacturer

  • Ateranvand_ej

    Medical Device

  • Ateranvand_ej

    The product is sterile through the use of aseptic processing techniques.

  • Ateranvand_ej

    The product is sterilised using irradiation.

  • Ateranvand_ej

    Do not use if the packaging is damaged.

  • Ateranvand_ej

    Single sterile barrier system

  • Ateranvand_ej

    Date of manufacture

  • Ateranvand_ej

    Keep away from sunlight

  • Ateranvand_ej

    Keep dry

  • Ateranvand_ej

    Temperature limitation. States the upper and lower limits for the storage temperature.

  • Ateranvand_ej

    Temperature limitation. States the upper and lower limits for the storage temperature.

  • Ateranvand_ej

    Caution. Consult instructions for use for warnings and precautions that cannot be presented on the medical device itself.

  • Ateranvand_ej

    Consult instructions for use

  • Ateranvand_ej

    Clean the wound

  • Ateranvand_ej

    Remove the plaster's protective paper (marked 1).

  • Ateranvand_ej

    Apply the plaster over the wound

  • Ateranvand_ej

    Remove the protective plastic top layer (marked 2).

  • Ateranvand_ej

    Remove plaster after 24 hours

  • Ateranvand_ej

    Clean the wound

  • Ateranvand_ej

    Apply the plaster over the wound

  • Ateranvand_ej

    Remove the plaster after 24 hours

  • Ateranvand_ej

    Renewable material

  • Ateranvand_ej

    Information on salvequick.com

  • Ateranvand_ej

    Information

  • Ateranvand_ej

    Importer. Indicates the entity importing the medical device into the locale

  • Ateranvand_ej

    Distributor. Indicates the entity distributing the medical device into the locale

  • Ateranvand_ej

    Contains hazardous substances

  • Ateranvand_ej

    Translation. To identify that the original medical device information has undergone a translation which supplements or replaces the original information

  • Ateranvand_ej

    Repackaging. To identify that a modification to the original medical device packaging configuration has occurred

  • Ateranvand_ej

    Patient information website. Indicates a website where a patient can obtain additional information on the medical product

  • Ateranvand_ej

    Country of manufacture

  • Ateranvand_ej

    Recyclable packaging

  • Ateranvand_ej

    Dispose in household trash

  • Ateranvand_ej

    Green dot. Indicates that the producer of the packaging has contributed financially to the recycling of that packaging

  • Ateranvand_ej

    Estimated sign. Nominal value (volume or weight)

  • Ateranvand_ej

    Limited quantity. Dangerous goods that are packaged in accordance with the Limited Quantity exemption.

  • Ateranvand_ej

    Reversed epsilon. Aerosol dispenser meets requirements in 75/324/EEC.

  • Ateranvand_ej

    Lot number and Expiry date printed on the bottom of the can

  • Ateranvand_ej

    Brim volume: (Brimful capacity, total capacity, for cans containing 100ml or more. Number depends on volume of can)