ASSE 6040 Final Test – NFPA 99 2021 edition

Which of the following systems shall not be permitted to be located in an outdoor enclosure?

All zone valves shall be installed such that a(n) _____ intervenes between the valve and the _____ that it controls.

An existing system that is not in strict compliance with NFPA 99 – 2021 edition shall be permitted to be continued in use, unless the _____ has determined such use constitutes a distinct hazard to life.

Medical air compressors which contain oil (not oil-less compressors) shall be monitored for gaseous hydrocarbons on a(n) _____ basis.

Vacuum filtration assemblies for medical vacuum central supply systems shall have a minimum of _____.

A 3/4″ medical gas valve for oxygen in the full open position would require a minimum Cv of _____ for compliance with NFPA 99.

Vacuum central supply systems shall have filtration located on the _____ side of the vacuum producer.

What are the colors assigned by the 2021 NFPA 99 standard to the following medical gases?(background/text colors)

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Ceiling and other downward facing station outlets/inlets shall use connector styles that are _____.

The installer 24-hour standing pressure test for positive pressure gases shall be witnessed by _____.

Pipe labels shall be located on the medical gas piping at intervals of not more than _____ ft.

Alarm indicators shall be tested _____ to determine if they are functioning properly, by personnel credentialed to the _____ standard.

CMT tubing used in NFPA 99 approved locations shall have an external coating that is _____.

Systems shall be deemed breached at the point of pipeline intrusion by physical separation, or by system component _____, _____, or _____.

General anesthesia and deep sedation are allowed on which categories of systems?

When alarm initiating devices are located remote from the building served (as with a bulk oxygen system), each signal shall be permitted to be connected to a junction box inside the building with a _____ set of wires.

Instrument air and nitrogen are considered to be:

The installer-performed initial pressure test shall be performed after the _____ test.

Positive pressure gas piping systems, which operate at other than standard gauge pressures, shall be labeled with the name of the gas and the _____.

Category 1 manifolds for gas cylinders (HP x HP) shall have two equal headers and each header shall have a minimum of __________ gas cylinder connections.

A zone valve shall be required for each _____.

Existing facilities shall:

Line pressure regulators used for a bulk cryogenic liquid system shall be of a _____ design.

_____ valves are considered to be optional valves.

Portions of systems that handle oxygen at pressures greater than _____ PSI shall contain no polymeric materials.

Medical gas piping shall be prohibited from installation in what areas?

The lines that serve a room or a group of rooms, and connect directly to zone valves are known as _____ lines.

The pressure for the 24-hour standing pressure test for category 1 oxygen piping is:

The medical air compressor intake shall be ___ ft. above the ground, and ___ ft. from any door or window, and ___ ft. from plumbing vents. 

The quality of instrument air shall be compliant with _____.

The standing vacuum test for vacuum performed by the installer shall be for _____ hours, and witnessed by the _____.

Cryogenic fluid central supply systems terminate:

A local alarm for high dew point shall be activated at -22°F for a(n) _____.

Labeling for zone valve box assemblies shall be visible and shall not be affixed _____.

When a bulk system reserve supply contents fall to _____ average supply, a _____ alarm shall be activated.

Testing of cryogenic fluid central supply systems shall be conducted by a party that meets the requirements of _____.

An emergency oxygen supply connection shall have a minimum of _____ ft. of clearance for connection of a temporary auxiliary source.

An alarm system that monitors the operation and condition of the source of supply, the reserve source, and the pressure in the main lines of each medical gas and vacuum piping system is a(n) ____________ alarm.

The installer standing pressure test for positive pressure medical gas piping shall allow a leakage rate of _____.

CMT tubing shall have all changes in direction made by _____.

Medical facilities which have activities, equipment or systems in whose failure is likely to cause major injury, death of patients or caregivers, shall meet the requirements of _____.

In-line check valves shall not have which of the following:

The person(s) designated as the Responsible Facility Authority shall be _________ to interpret, implement and advise on this Code.

Source equipment shall be labeled for _____.

How many master alarm contacts must a newly installed EOSC have?

All _____ central supply systems shall be provided with an auxiliary source connection.

Control equipment for final line pressure regulators, relief valves, and separate piped distribution networks operating at different pressures, that is physically remote from the supply system shall be installed within a ______________________.

Category 1 spaces (excluding anesthetizing locations) shall have area alarm sensors installed _____.

Instrument air supply source systems shall supply a minimum pressure of _____.

The maximum allowable temperature for cylinder storage is _____.

Cylinder relief valves shall be constructed of _____.

A minimum one-hour fire rating shall be required for _____.

Hoses of flexible connectors in manufactured assemblies shall be labeled with _____.

Manifolds for cryogenic liquid containers which are stored outdoors shall have minimum separation distances specified by _____.

Non-stationary manufactured assemblies which employ flexible connections between the user terminal and the piping system shall be tested for leaks per the manufacturer’s recommendation, or every _____ months.

All cryogenic fluid central supply systems now require an auxiliary source connection point located on the patient side of the source valve. What is the minimum size of this connection?

Central supply systems using CO2 or N2O cylinders shall be prevented from reaching temperatures lower than:

Medical vacuum inlets shall draw__________SCFM, without reducing the vacuum pressure below _______ at any adjacent station inlet.

Risk categories are classified by the health care facility’s _____.

Piping distribution systems shall be inspected by _____ prior to being concealed in walls, ceilings and chases.

An oxygen enriched atmosphere is defined (by NFPA 99) as an atmosphere in which the concentration of oxygen exceeds _____ percent.

Labels for shut-off valves shall be updated________________________.

A minimum of three connections is required on a(n) _____ header.

A vessel which contains gases in a liquid form is a _____, which dispenses the gas at _____.

When an alarm initiating device is disconnected from a master or area alarm system, the system shall activate a(n) _____ alarm.

A manifold for cryogenic liquid containers which is stored outdoors shall have a minimum separation distance of _____ from combustible materials.

Medical facilities which have activities, equipment or systems in whose failure is likely to cause minor injury to patients or caregivers, shall meet the requirements of _____.

Medical facilities which have activities, equipment or systems in whose failure is not likely to cause injury, but may cause discomfort to patients or caregivers, shall meet the requirements of _____.

The Responsible Facility Authority must be qualified to ASSE 6010, 6020, 6030 or 6040 and must be _________________ on the specific equipment and design of that facility.

Nitrogen and instrument air are known as _____________ gases.

___________ shall not be introduced into the medical vacuum or WAGD system for disposal.

The ___________________ shall be responsible for developing and enforcing the permit-to-work rules for the piped medical gas and vacuum systems.

A facilities permit-to-work system for piped medical gases should ensure that all individuals performing the work hold the appropriate qualifications.

Functional testing is not required if only the front body of an outlet is replaced.

Medical-surgical vacuum sources shall be located in a room designed to maintain the ambient temperature range as stipulated by:

The chapter in NFPA 99 that covers the different risk categories and when a documented risk assessment is required is chapter_____.

Medical air sources shall be used only for_________________.