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manufacturer

authorized representative in european community

date of manufacture

indicates manufacturer declaration that the product complies with the essential requirements of the relevant european health, safety and environmental protection legislation.

european medical devices directive 93/42/eec of 14 june 1993 (as amended by directive 2007/47/ec). as described in article 17 of the directive.

indicates the authorized representative in the european community.

ss-en iso 15223-1:2016 medical devices – symbols to be used with medical device labels, labelling and information to be supplied – part 1: general requirements (iso 15223-1:2016) ref no: 5.1.2

indicates the date when the medical device was manufactured.

ss-en iso 15223-1:2016 medical devices – symbols to be used with medical device labels, labelling and information to be supplied – part 1: general requirements (iso 15223-1:2016) ref no: 5.1.2

use-by date

batch code

catalogue number

indicates the date after which the medical device is not to be used.

ss-en iso 15223-1:2016 medical devices – symbols to be used with medical device labels, labelling and information to be supplied – part 1: general requirements (iso 15223-1:2016). ref no: 5.1.4

indicates the manufacturer’s batch code so that the batch or lot can be identified.

ss-en iso 15223-1:2016 medical devices – symbols to be used with medical device labels, labelling and information to be supplied – part 1: general requirements (iso 15223-1:2016). ref no: 5.1.5

indicates the manufacturer’s catalogue number so that the medical device can be identified.

ss-en iso 15223-1:2016 medical devices – symbols to be used with medical device labels, labelling and information to be supplied – part 1: general requirements (iso 15223-1:2016. ref no: 5.1.6)

ce-mark

ce-mark with notified body number

medical device

indicates manufacturer declaration that the product complies with the essential requirements of the relevant european health, safety and environmental protection legislation.

european medical devices directive 93/42/eec of 14 june 1993 (as amended by directive 2007/47/ec). as described in article 17 of the directive.

indicates manufacturer declaration that the product complies with the essential requirements of the relevant european health, safety and environmental protection legislation.

european medical devices directive 93/42/eec of 14 june 1993 (as amended by directive 2007/47/ec) as described in article 17 of the directive

indicates that the device is a medical device as defined in mdr 2017/745

sterilized using ethylene oxide

sterilized using irradiation

sterilized using steam or dry heat

indicates a medical device that has been sterilized using ethylene oxide.

ss-en iso 15223-1:2016 medical devices – symbols to be used with medical device labels, labelling and information to be supplied – part 1: general requirements (iso 15223-1:2016). ref no: 5.2.3

indicates a medical device that has been sterilized using irradiation.

ss-en iso 15223-1:2016 medical devices – symbols to be used with medical device labels, labelling and information to be supplied – part 1: general requirements (iso 15223-1:2016). ref no: 5.2.4

indicates a medical device that has been sterilized using steam or dry heat.

ss-en iso 15223-1:2016 medical devices – symbols to be used with medical device labels, labelling and information to be supplied – part 1: general requirements (iso 15223-1:2016). ref no: 5.2.5

non-sterile

do not use if package is damaged

keep away from sunlight

indicates a medical device that has not been subjected to a sterilization process.

ss-en iso 15223-1:2016 medical devices – symbols to be used with medical device labels, labelling and information to be supplied – part 1: general requirements (iso 15223-1:2016). ref no: 5.2.7

indicates a medical device that should not be used if the package has been damaged or opened.

ss-en iso 15223-1:2016 medical devices – symbols to be used with medical device labels, labelling and information to be supplied – part 1: general requirements (iso 15223-1:2016). ref no: 5.2.8

indicates a medical device that needs protection from light sources.

ss-en iso 15223-1:2016 medical devices – symbols to be used with medical device labels, labelling and information to be supplied – part 1: general requirements (iso 15223-1:2016). ref no: 5.3.2

keep dry

temperature limit

do not re-use

indicates a medical device that needs to be protected from moisture.

ss-en iso 15223-1:2016 medical devices – symbols to be used with medical device labels, labelling and information to be supplied – part 1: general requirements (iso 15223-1:2016). ref no: 5.3.4

indicates the temperature limits to which the medical device can be safely exposed.

ss-en iso 15223-1:2016 medical devices – symbols to be used with medical device labels, labelling and information to be supplied – part 1: general requirements (iso 15223-1:2016). ref no: 5.3.7

indicates a medical device that is intended for one use, or for use on a single patient during a single procedure.

ss-en iso 15223-1:2016 medical devices – symbols to be used with medical device labels, labelling and information to be supplied – part 1: general requirements (iso 15223-1:2016). ref. no: 5.4.2

consult instructions for use

caution

contains or presence of natural rubber latex

indicates the need for the user to consult the instructions for use.

ss-en iso 15223-1:2016 medical devices – symbols to be used with medical device labels, labelling and information to be supplied – part 1: general requirements (iso 15223-1:2016). ref. no: 5.4.3

indicates the need for the user to consult the instructions for use.

for important cautionary information such as warnings and precautions that cannot, for a variety of reasons, be presented on the medical device itself.ss-en iso 15223-1:2016 medical devices – symbols to be used with medical device labels, labelling and information to be supplied – part 1: general requirements (iso 15223-1:2016). ref. no: 5.4.4.

indicates the presence of natural rubber or dry natural rubber latex as a material of construction within the medical device or the packaging of a medical device.

ss-en iso 15223-1:2016 medical devices – symbols to be used with medical device labels, labelling and information to be supplied – part 1: general requirements (iso 15223-1:2016) ref. no: 5.4.5.

this way up

recycle

to indicate correct upright position of the transport package.

iso 7000 graphical symbols for use on equipment — registered symbols. ref no: 0623.

iso 7001 graphical symbols -- public information symbols. ref. no: pi pf 066