NovoPen
®
3
Novo Nordisk A/S
2880 Bagsvaerd
Denmark
17
Remember
■
Always have extra insulin of the same type(s) you use
available for alternative administration in case your
NovoPen
®
3 gets lost or damaged.
■
Do not try to repair a faulty NovoPen
®
3.
■
NovoPen
®
3 must only be used in the way described in this
booklet. The manufacturer will not be responsible for any
problems you have with the equipment if instructions are
not followed.
■
Novo Nordisk will replace a NovoPen
®
3 if:
■
you return the pen to your supplier within a year of
getting it,
■
you enclose any documents you were given when you got
the pen, and
■
Novo Nordisk can inspect the pen and confirm that it
is faulty.
LOT
6
8
NovoPen
®
3
Cap
Inspection window
Piston rod
Dosage selector
Push button
NovoFine
®
Outer needle cap
Inner needle cap
Needle
Protective tab
Penfill
®
Rubber membrane
Colour-coded cap
Glass ball (for insulin
suspensions only)
Coloured band
White bar code band
Rubber stopper
(plunger)
Return mechanism
Dosage indicator
window
LOT number
Residual scale
Residual scale
window
Penfill
®
holder
Mechanical section
NovoPen
®
3 insulin pen should only be used in combination with
products that are compatible therewith and allow the pen to
function safely and effectively.
Penfill
®
cartridges and NovoFine
®
needles are designed to be used
with NovoPen
®
3 insulin pen.
NovoPen
®
, Penfill
®
and NovoFine
®
are trademarks owned by
Novo Nordisk A/S.
The CE-mark on a medical device indicates that the product conforms with the
provisions in the EC Directive for Medical Devices 93/42/EEC. NovoPen
®
3 fullfils the
specification limits for dose accuracy according to ISO/DIS 11608 -1.2 Pen-Injectors
for Medical use, Part 1: Requirements and test methods.
