Glossary Of Symbols And Product Graphics; Symbols - Hologic Acessa ProVu User Manual

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Acessa
ProVu System User's Guide
®

20. Glossary of Symbols and Product Graphics

20.1.

Symbols

Standard
Symbol
Symbol
Reference
Number
EN 50419
US 21 CFR
801.109
IEC 60601-
1:2012
Table D.1,
Symbol 20
IEC 60417-
5331: 2002
IEC 60417 -
5036
ISO 15223-
1:2016
5.4.2
ISO 15223-
1:2016
5.1.5
ISO 15223-1:
2016
5.1.7
USB
Implementors
Forum, Inc.
ISO 15223-1,
50C
Clause 5.3.8
-10C
CO 20-131 Revision: C
Symbol Title
Symbol
/Description
Recycle: Electronic
Equipment / Do Not
Throw Away.
Prescription Only /
Device restricted to use
by or on the order of a
physician.
BF Type Applied Part /
To identify a type BF
applied part complying
with IEC 60601-1.
Not Anesthetic Proofed
/ Not suitable for use
with flammable
anaesthetics!
Warning: Electricity /
Warning dangerous
voltage.
Single Use only /
Indicates medical device
that is intended for one
use, or for use on a
single patient during a
single procedure.
Lot Identification /
Indicates the
manufacturer's batch
code so that the batch
or lot can be identified.
Serial Number /
Indicates
manufacturer's serial
number so specific
medical device can be
identified.
USB Port /External
interface to support
data transfer to
peripheral devices.
Storage temperature
range / Indicates range
of temperature the
medical device can be
safely exposed.
10
Standard
Symbol
Symbol Title/ Description
Reference
Number
Alternating Current / To indicate on
IEC 60417-
the rating plate that the equipment is
5032:2002
suitable for alternating current only;
to identify relevant terminals.
Radio Frequency /To indicate
generally elevated, potentially
hazardous, levels of nonionizing
radiation, or to indicate equipment or
IEC 60417-
systems e.g. in the medical electrical
5140:2003
area that include RF transmitters or
that intentionally apply RF
electromagnetic energy for diagnosis
or treatment.
Potential Equalization Terminal / To
identify the terminals which, when
connected together, bring the various
IEC 60417-
parts of an equipment or of a system
5021:2002
to the same potential, not necessarily
being the earth (ground) potential,
e.g. for local bonding.
IEC 60601-
1:2012
Follow Instructions for Use / Refer
Table D.2,
to instruction manual/booklet.
Symbol 10
ISO 15223-
Date of Manufacture / Indicates the
1:2016
date when the medical device was
5.1.3
manufactured.
Fuse Rating / To identify fuse boxes
IEC 60417-
5016: 2002
or their location.
Catalogue or Model Number /
ISO 15223-
Indicates the manufacturer's
1:2016
catalogue number so that the
5.1.6
medical device can be identified.
IEC 60417-
Monitor / To identify the terminals
505: 2002
and controls for a television monitor.
Use by / Indicates the date after
ISO 15223-
1:2016
which the medical device is not to be
5.1.4
used (YYYY-MM-DD).
ISO 15223-
Storage humidity range / Indicates
90
1, Clause
range of humidity to which the
5.3.7
medical device can be safely exposed.
PL-01-0040
39

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