Appendix
NXT Owner’s Manual, NXT-UM01, MAN2010
110
Appendix B: Symbols Glossary
Authorized
Representative in the
European Community
(5.1.2)
1
:
Indicates the
manufacturer’s device
representative in the
European
Community.
SGS certification -
certified to U.S. and
Canadian safety
standards.
Date of Manufacture
(5.1.3)
1
:
Indicates the date of
device manufacture.
Manufacturer (5.1.1)
1
:
Indicates the device
manufacturer.
Consult Instructions for
Use (5.4.3)
1
:
Manufacturer
recommends
consultation of
Instructions for Use.
Read Operator’s Manual
(M002)
3
:
Indicates user must
refer to Owner’s
Manual.
Lot - Batch Code
(5.1.5)
1
:
Indicates the batch or
lot code for
identification and
tracking purposes.
Catalogue Number
(5.1.6)
1
:
Indicates the device
model or catalogue
number.
Serial Number
(5.1.7)
1
:
Indicates unique
device serial number
for device
traceability.
Class II Equipment
(Table D.1, 9)
2
:
Identifies Class II
Medical Electrical
Equipment.
Type BF Applied Part
(Table D.1, 20)
2
:
Identifies a type BF
applied part complying
with IEC 60601-1.
Use-by Date (5.1.4)
1
:
Indicates date after
which use is prohibited.
Sterile (5.2.1)
1
:
Indicates a sterile
device.
Sterilized Using
Irradiation (5.2.4)
1
:
Indicates method of
sterilization used as
irradiation.
Alternating Current
(Table D.1, 1)
2
:
Indicates use of
Alternating Current.
Direct Current
(Table D.1, 1)
2
:
Indicates use of Direct
Current.
Non-ionizing
electromagnetic
Radiation (5140)
5
:
Radio Frequency (RF)
Transmitting Device
Indicates presence of
RF transmitters.
Keep Dry (5.3.4)
1
Indicates a device
requiring protection
from moisture.
Power Off
(Table D1, 13)
2
:
Indicates power off
control.
Power ON
(Table D.1, 14)
2
:
Indicates a stable
position power ‘on’
control.
Do Not Re-Use
(5.4.2)
1
:
Medical device
intended for single
use, on a single
patient, during a
single procedure.
Safety Label, No
Pushing (P017)
3
:
To prohibit pushing
against a specified
device.
Safety Label, No Sitting
(P018)
3
:
Indicates sitting on the
identified surface is
prohibited.
Safety Label, No
Stepping on Surface
(P019)
3
:
To prohibit stepping on
a specified surface.
Humidity Limitation
(5.3.8)
1
:
Indicates the
humidity range to
which the medical
device can be safely
exposed.
Temperature Limit
(5.3.7)
1
:
Indicates the
temperature limit to
which the medical
device can be safely
exposed.
Fragile, handle with
care (5.3.1)
1
:
Indicates the
medical device can
be broken or
damaged by not
handling carefully.
This way up (0623)
4
:
Indicates the direction
which the box should
remain oriented (stored
or shipped) to avoid
potential damage to
the device.
Handle with Care
(No Associated
Standard)
Indicates the medical
device can be broken
or damaged by not
handling carefully
General Battery
(5001B)
4
:
Identifies a device
related to the power
supply by battery.