Manufacturer
Indicates the medical device manufacturer, as defined in EU Directives 90/385/EEC, 93/42/EEC and 98/79/EC
5.1.1
Authorized Representative in European Community
Indicates the authorized representative in the European Community
5.1.2
Date of Manufacture
Indicates the date when the medical device was manufactured
5.1.3
Use-by Date
Indicates the date after which the medical device is not to be used
5.1.4
Batch Code
Indicates the manufacturer's batch code so that the batch or lot can be identified
5.1.5
Importer
Indicates the entity importing the medical device into the locale
5.1.8
Sterilized Using Steam Heat
Indicates a medical device that has been sterilized using steam heat
5.2.5
Do Not Use if Package is Damaged and Consult Instructions for Use
Do Not Use if Package is Damaged and Consult Instructions for Use
5.2.8
Single sterile barrier system
Indicates a Single Sterile Barrier System
5.2.11
Keep away from Sunlight
Indicates a medical device that needs protection from light sources
5.3.2
Do not re-use
Indicates a medical device that is intended for one use
5.4.2
Consult Instructions for Use
Indicates the need for the user to consult the instructions for use
5.4.3
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
5.4.4
Contains Hazardous Substances
Indicates a medical device that contains substances that can be carcinogenic, mutagenic, reprotoxic (CMR), or substances with endocrine disrupting properties
5.4.10
Medical Device
Indicates the item is a medical device
5.7.7
