WARNING: Never advance the LiquID device into a vessel
without a leading guidewire or without confirming location
using fluoroscopic guidance. Vessel injury may result.
WARNING: Never advance the LiquID device more than
10cm beyond the guide catheter tip. The LiquID device
may become lodged in the guide catheter making it
difficult to remove.
WARNING: Never advance the LiquID device into a
vessel with an effective diameter less than 2.5mm. Vessel
injury, ischemia, and/or occlusion may result. If pressure
in a vessel dampens after inserting the LiquID device,
withdraw the LiquID device immediately.
5. Insert the interventional device over the guidewire,
through the hemostasis valve, and into the guide catheter.
6. Close the hemostasis valve. Perform the interventional
procedure according to the instructions provided by
the interventional device manufacturer.
7. Remove all interventional devices.
8. Remove the LiquID device ensuring that the hemostasis
valve is fully open prior to retracting the LiquID device
lumen through the hemostasis valve.
9. Dispose of device and packaging in accordance with
hospital administrative and local government policy.
Notice
If a serious incident related to the LiquID device has occurred,
report the incident to the manufacturer and the local
government competent authority.
Batch code
Catalog number
Medical Device
Sterilized using ethylene oxide
EU authorized representative
Legal manufacturer
Prescription only
Consult instructions for use
Date of manufacture
Use by date
Do not re-use
Keep away from rain
Keep away from sunlight
Non pyrogenic
Do not use if package is damaged
Do not resterilize
Inner diameter
3