Bayer HealthCare CERTEGRA MEDRAD Stellant FLEX Operation Manual page 13

Operation Manual 2 - 5
Keep Dry (ISO 15223-1, 5.3.4)
Fragile, Handle With Care (ISO 15223-1, 5.3.1)
Indicates that this device conforms to the requirements of the European Medical
Device Directive 93/42/EEC.
Identifies a type BF applied part complying with IEC 60601-1 standards. (IEC 60417,
5333)
Medical - General Medical Equipment
As To Electrical Shock, Fire, and Mechanical Hazards Only
In accordance with ANSI/AAMI ES60601-1 (2005)
+ AMD 1 (2012) CAN/CSA-C22.2 No. 60601-1 (2014)
See accompanying documentation. This symbol indicates the user shall refer to the
instructions-for-use to ensure safe operation. (ISO 7010, M002)
Indicates the injection system is Class 1 medical equipment as defined by IEC 60601-
CLASS 1
1 standards.
Class II Equipment, Double Insulated (IEC 60417, 5172)
IPX1 Code that specifies the degree of protection provided by the enclosure against
vertically falling water drops (IEC 60529)
Indicates separate collection for Electrical and Electronic Equipment per Directive
2002/96/EC. Refer to the following website for additional information:
www.weee.bayer.com (EN 50419, Fig. 1)
Indicates that this product contains certain toxic or hazardous substances or
elements and can be used safely during its environmental protection use period,
indicated by the number in the center of the logo. This product should be recycled
immediately after its environmental protection use period has expired.
Identifies an on/off switch for equipment. (IEC TR 60878, 5009)
Identifies a computer network. (IEC TR 60878, 5988)
Identifies a power supply. (IEC TR 60878, 5534)