 | Manufacturer | Indicates the manufacturer of the medical device as defined in Regulation (EU) 2017/745. This symbol of the black factory (manufacturer) shall be usedin close proximity to the name and address of the manufacturer. |
 | Useable until | Indicates the date after which the me-dical product should no longer be used. |
 | Batch number | Specifies the manufacturer’s serial code in order to identify the series or batch. The manufacturer’s batch number is indicated immediately next to this symbol. |
 | Period-after-opening | Indicates the period of time during which the product can be used safely after first opening. |
 | Protect from sunlight | Indicates a medical device that must be protected from sunlight. |
 | Read the instructions for use | Reference to the necessity for the user to consult the instructions for use. |
 | Medical Device | Indicates that it is a medical device according to Regulation (EU) 2017/745 on medical devices. |
 | CE MARKING OF CONFORMITY | Indicates conformity with applicable European Union legislation and, where applicable, involvement of a notified body. |
 | Article number | Indicates the manufacturer’s article number in order to identify the medical device. |
| XXX-XX/JJJJ/MM/DD | LSP-Nr/date of issue IFU | Indicates the date of issue of the instructions for use and their revision number. |
