Glossary Of Symbols - Cooper Surgical Inca 44-27 Serie Instrucciones De Uso

INCA Complete Set, Replacement Set and Accessory Pack
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GLOSSARY OF SYMBOLS

Ref # Symbol Title
Catalogue
5.1.6
number
5.1.5 Batch code
Date of
5.1.3
manufacture
5.1.4 Use-by date
Sterilized using
5.2.3
ethylene oxide
Not made with
5.4.5,
Annex natural rubber
B.2 latex
Do not re-use
5.4.2
Do not use if
package is
5.2.8
damaged
Consult
instructions for
5.4.3
use
Authorized
representative
5.1.2
in the European
Community
Manufacturer
5.1.1
n.a. Prescription device
Not made with
PHT
n.a. phthalates
DEHP FREE
n.a. Medical Device
Product conforms
to the Medical
n.a.
Device Directive
93/42/EEC
Standard
Description Development
Organization
Indicates the manufacturer's
catalogue number so that
ISO 15223-1
the medical device can be
identifi ed.
Indicates the manufacturer's
batch code so that the batch ISO 15223-1
or lot can be identifi ed.
Indicates the date when
the medical device was ISO 15223-1
manufactured.
Indicates the date after
which the medical device is ISO 15223-1
not to be used.
Indicates a medical device
that has been sterilized ISO 15223-1
using ethylene oxide.
Indicates that natural
rubber latex was not used
in the manufacturing of the ISO 15223-1
product, its container, or its
packaging.
Indicates a medical device
that is intended for one use,
ISO 15223-1
or for use on a single patient
during a single procedure.
Indicates a medical device
that should not be used
ISO 15223-1
if the package has been
damaged opened.
Indicates the need for
the user to consult the
ISO 15223-1
instructions for use.
Indicates the authorized
representative in the
ISO 15223-1
European Community.
Indicates the medical device
manufacturer, as defi ned in
ISO 15223-1
EU Directive 90/385/EEC,
93/42/EEC and 98/79/EC.
Caution: Federal law
(USA) restricts this device
to sale by or on the order 21 CFR 801.109
of a licensed healthcare
practitioner.
n.a. n.a.
Medical Device n.a.
Signifi es European technical
n.a.
conformity.
4
(English)