Versions - Atmos MEDAP FINA VAC T 50 Operating Instructions Manual

Contraindications:
The product is:
Sterility:
Single-use product /
reprocessing:
1.6.4

Versions

The connection of the FINA VAC T 50 to the terminal unit for vacuum depends on the model
being used:
Version A: Tapping unit with integrated gas pin
• FINA VAC T 50 is fitted directly to the terminal unit.
Version B: Tapping unit with rail clamp and NIST connection
• FINA VAC T 50 is designed for mounting onto a 25 x 10 mm equipment rail and is supplied via
a NIST connection with vacuum from a terminal unit connected using a connection tube with
gas probe.
Products and accessories are only permitted with ISO colour coding. In Germany, Austria and
Switzerland, products with neutral colour coding are also permitted.
The product is available in the following versions:
• FINA VAC T 50 Wall DIN (REF 5752 3747)
• FINA VAC T 50 Equipment rail (REF 5752 3748)
The FINA VAC T 50 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 vacuum extraction
• For the aspiration of flammable or explosive liquids
• For the aspiration of smoke that is generated during HF and
laser surgery
• For surgical aspiration
• For bronchial aspiration
• For thoracic drainage without additional use of a water
manometer
• In combination with disposable thoracic drainage systems which
require a flow higher than 12 l/min or a vacuum higher than
−5 kPa
• With central gas supply systems with supply pressures other
than −100 kPa to −60 kPa
Active
Not a sterile product
The device and parts of the accessories are reusable. For
information on reprocessing, cleaning and disinfection, please see
the operating instructions.
NOTE
The products are supplied with ISO coding. The scope of delivery includes a label
for neutral colour coding.
1
Introduction
Basic requirements
11
GA 5752 3075 GB 13