Product
Informa
tion
63
62
These symbols are found on the
SKYTROFA Auto-Injector, the packaging,
and the Instructions for Use.
Manufacturer.
Unique serial number of
SKYTROFA Auto-Injector.
Manufacturer catalogue number for
identification.
Manufacturer batch code for
identification.
YYYY-MM-DD
Expiration date.
See Instructions for Use.
Applied parts
SKYTROFA Auto-Injector is a type BF
device and provides protection against
electrical shock and electrical current
leakage.
Applied parts on the device are the
green top, the housing, and the button.
Warning!
When this symbol is seen, safety
instructions must be followed.
Rx only Caution: Federal law restricts this device
for sale by or on the order of a physician.
Symbols
30°C
86°F
15°C
59°F
Operation temperature.
40°C
104°F
-10°C
14°F
Storage & Transportation temperature.
Keep dry.
2460
SKYTROFA Auto-Injector complies
with the requirements of The Medical
Device Directive (MDD 93/42/EEC)
and the RoHS (Restriction of Hazardous
Substances) directive (2011/65/EU).
SKYTROFA Auto-Injector contains
electrical and electronic components,
including a battery that cannot be
replaced, and must not be disposed of
using standard waste collection.
SKYTROFA Auto-Injector packaging
material is suitable for household waste.
d
DC (Direct Current).
(01) 05713495000077
(10) B00052690
(17) 211031
(21) 18110000123456
The Unique Device Identifier (UDI) that appears on
the carton is shown by a barcode and human
readable format:
(01) Device Identifier
(10) Batch Number
(17) Expiry date in YYMMDD format
(21) Serial Number
