Product Description - natus Echo-Screen III Instrucciones De Uso

Standard
Symbol
Reference
ISO 7000
Symbol 1135
combined with a
battery chemistry
symbol to differentiate
battery type
21 CFR Part
801.109(b)(1)
ISO 15223-1
Symbol 5.4.5
LATEX
(Reference Annex
B for the general
prohibition symbol)
2012/19/EU
ISO 15223-1
Symbol 5.1.1
ISO 15223-1
Symbol 5.1.2
ISO 15223-1
Symbol 5.1.3
ISO 15223-1
Symbol 5.1.6
ISO 15223-1
Symbol 5.1.7
ISO 15223-1
Symbol 5.4.3
Annex A #A.15
ISO 15223-1
Symbol 5.4.4
IEC 60601-1
Table D.1 #10
ISO 60601-1
Table D.2 #2
ISO 15223-1
Symbol 5.2.8
ISO 15223-1
Symbol 5.3.7
ISO 15223-1
Symbol 5.3.8
ISO 15223-1
Symbol 5.3.9
Product Part
Numbers
010041
Standard Title
Lithium-ion Recycling Symbol
Labeling-Prescription devices
Medical devices — Symbols to be used
with medical device labels, labelling and
information to be supplied.
Waste Electrical and Electronic Equipment
(WEEE)
Medical devices — Symbols to be used
with medical device labels, labelling and
information to be supplied.
Medical devices — Symbols to be used
with medical device labels, labelling and
information to be supplied.
Medical devices — Symbols to be used
with medical device labels, labelling and
information to be supplied.
Medical devices — Symbols to be used
with medical device labels, labelling and
information to be supplied.
Medical devices — Symbols to be used
with medical device labels, labelling and
information to be supplied.
Medical devices — Symbols to be used
with medical device labels, labelling and
information to be supplied.
Medical devices — Symbols to be used
with medical device labels, labelling and
information to be supplied.
Medical electrical equipment — Part 1:
General requirements for basic safety and
essential performance.
Medical electrical equipment — Part 1:
General requirements for basic safety and
Essential performance.
Medical devices — Symbols to be used
with medical device labels, labelling and
information to be supplied.
Medical devices — Symbols to be used
with medical device labels, labelling and
information to be supplied.
Medical devices — Symbols to be used
with medical device labels, labelling and
information to be supplied.
Medical devices — Symbols to be used
with medical device labels, labelling and
information to be supplied.
Label Part Numbers
021520
Symbol Title
Recycling identification
mark
Prescription only
Not made with Natural
Rubber Latex
Disposal at end
of operating life
instructions
Manufacturer
Authorized
representative in the
European Community
Date of manufacture
Catalogue number
Serial number
Consult instructions for
use
Caution: Read
all warnings and
precautions in
instructions for use
General warning sign
Do not use if package
is damaged
Temperature limit
Humidity limitation
Atmospheric pressure
limitation

Product Description

• Do not incinerate.
• Do not expose to high temperature.
• Do not disassemble.
• Do not short terminals.
Explanation
Indicates the battery composition for
recycling purposes.
Indicates the product is authorized for
sale by or on the order of a licensed
healthcare practitioner.
Indicates a medical device that is not
made with natural rubber latex.
Indicates that electrical and electronic
equipment waste should not be
discarded together with unseparated
waste but must be collected separately.
Indicates the medical device
manufacturer.
Indicates the Authorized representative
in the European Community.
Indicates the date when the medical
device was manufactured.
Indicates the manufacturer's catalogue
number so that the medical device can
be identified.
Indicates the manufacturer's serial
number so that a specific medical
device can be identified.
Indicates an instruction to consult an
electronic instructions for use (eIFU).
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.
Indicates a hazard of potential personal
injury to patient or operator.
Indicates a medical device that should
not be used if the package has been
damaged or opened.
Indicates the (storage) temperature
limits to which the medical device can
be safely exposed.
Indicates the range of (storage)
humidity to which the medical device
can be safely exposed.
Indicates the acceptable upper and
lower limits of atmospheric pressure for
transport and storage.
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