10
Clinical Limitations/Restrictions
Use of the IPV®-2C is limited to individuals who have received proper training.
For invasive applications or patients supported by Continuous Mandatory Ventilation (CMV).
WARNING: Due to the therapeutic nature of these devices, they do not have
disconnect alarms . Consequently, the patient MUST be under continuous observation
by a clinician.
WARNING: When used on a patient with an articial airway (i.e. endotracheal or
tracheostomy tube) a clinician must be present so that a one-to-one relationship exists.
These devices enhance secretion clearance. Patients must be assessed pre- and
post-treatment for a reduced vital capacity (FRC) or the need for assistance in clearing
airway secretions. Partial deation of the cu during therapy may be necessary;
re-ination per hospital protocol post-therapy.
WARNING: Because pulmonary alveoli cannot be ventilated when their transmitting
airways are obstructed, suction should be performed as necessary.
Document Symbols
NON
STERILE
LATEX
PHT
DEHP
DIBP
DBP
BBP
i
C
M
N
D
h
g
y
WARNING
CAUTION
Read the manual
before use
CE marking
Manufacturer
Manufacture Date
Non-Sterile
Does Not Contain
the Phthalate
Plasticizers DEHP,
DIBP, DBP, or BBP
Type BF Applied Part
Single Patient Use
Prescription Only
Catalog Number
Lot Number
European
Representative
Not Made with
Natural Rubber Latex
Disposal
NOTE: A WARNING icon indicates a risk of injury to patient or operator.
A CAUTION icon indicates a risk of equipment damage.