INION FreedomPin Mode D'emploi page 3

• Neurovascular injuries can occur due to surgical trauma.
• Implantation of foreign materials can result in an inflammatory response or allergic reaction. Transient local fluid accumulation may occur
in sterile circumstances.
STERILITY
The INION FreedomPin™ implants and INION FreedomPin™ Kits have been sterilized with ionizing irradiation. Use immediately after
opening the sterile seal. Use only devices that are contained in unopened and undamaged packages. For single use only. DO NOT re-
sterilize or re-use! If the device is re-sterilized or re-used, the properties of the implant will be affected, and the safety and efficacy cannot
be guaranteed. DO NOT use implant beyond the expiration date on the label!
STORAGE
Store at room temperature (15 to 30°C / 59 to 86°F) at a normal relative humidity. Product should not exceed a maximum temperature
defined on the indicator. Do not use if the indicator dot is black.
CAUTION
Federal law (USA) restricts this device to sale by or on the order of a licensed physician.
MANUFACTURER
INION Oy
Lääkärinkatu 2
33520 Tampere
Finland
Tel. +358 10 830 6600
Fax +358 10 830 6601
info@inion.com
www.inion.com
2797
®
Inion is a registered trademark of Inion Oy.
SYMBOLS USED IN LABELING
Manufacturer
Catalogue number
Date of manufacture
Sterilized using irradiation
Storage temperature range
Caution, consult accompanying documents
Lot number
Use by
CE marked product
Keep dry
Do not re-use