54
Dispose of according to WEEE
DO NOT THROW IN
GENERAL RUBBISH
DISPOSAL/TRASH! –
Waste Electronic
Equipment
EN 50419
Directive 2012/19/EU,
Annex IX
Serial number
Indicates the
manufacturers serial
number so that a
specific medical device
can be identified
ISO 15223 – 1. Clause 5.1.7
ISO 7000 – 2498
Manufactured by
Indicates the device
manufacturer (*Note –
Date of manufacture,
name and address of
manufacturer can be
combined in one
symbol)
ISO 15223 – 1. Clause 5.1.1
ISO 7000 – 3082
Manufacture date
Indicates the date
when the medical
device was
manufactured
ISO 15223-1. Clause 5.1.3
ISO 7000 – 2497
FDA 21 CFR 801
Magnetic Resonance (MR)
unsafe
3.1.14: An item which
poses unacceptable
risks to the patient,
medical staff or other
persons within the MR
environment
ASTM F2503-20. Table 2,
Symbol 7.3.3; 7.4.9.1; Fig.9
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
ISO 15223-1 Clause 5.4.4
ISO 7000 – 0434A
FDA 21 CFR 801
Prescription only
Caution: Federal Law
restricts this device to
sale by or on the order
of a physician
FDA 21 CFR 801.109
Temperature limit
Indicates the
temperature limits to
which the medical
device can be safely
exposed
ISO 15223 – 1. Clause 5.3.7
ISO 7000 – 0632
