Atmos MEDAP FINA DFLOW, Руководство по эксплуатации

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Introduction
Basic requirements
GA 5752 2804 GB 18
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Patient groups: Patients of all ages
Application organ: Lung
Application time: For continuous operation; in practice, short-term use on the patient
(< 30 days)
Application site: The application site is the clinical environment and doctor’s
practices which have a central oxygen / compressed air system.
The application of the product may only be performed by medically
trained and instructed staff.
Contraindications: The FINA FLOW may not be used for the following purposes:
• Outside the medical sector
• In MR areas
• In the home care sector
• Being operated directly by the patient
• For exclusive respiration
• With central gas supply systems having supply pressures other
than 500 kPa ± 10%
• When applying oxygen in its function as a medication, it is abso-
lutely necessary to measure the flow rate.
The product is: Not active
Sterility: Not a sterile product
Single-use product /
reprocessing:
The device and parts of the accessories are reusable. For
information on reprocessing, cleaning and disinfection, please see
the operating instructions.
1.5.4 Versions of FINA FLOW / DFLOW flowmeter
The connection of the tapping unit to oxygen or compressed air depends on the model being
used:
Version A: Tapping unit with integrated gas pin
• FINA FLOW is fitted directly to the terminal unit.
Version B: Tapping unit with rail clamp and NIST connection
• FINA FLOW is designed for mounting onto a 25 x 10 mm equipment rail and is supplied via a
NIST connection with oxygen or compressed air from a terminal unit connected using a con-
nection tube with gas probe.
Products and accessories are only permitted with the ISO colour coding. In Germany, Austria and
Switzerland, products with neutral colour coding are also permitted.
NOTE
The products are supplied with ISO coding. The scope of delivery includes a label
for neutral colour coding.