SHELF LIFE OF APPLIANCES &PROPER OPERATING
The filter and sterilization components of the device have the following time limits for proper operation and if you carry ou
the devices. The appliance must not be operated outdoors or in damp rooms, with a hu
appliances using gas. In environments with temperature fluctuations, as this can lead to water condensation inside.
3-5 weeks
.
APPLIANCE ACCESSORIES
Dust prefilter
Activated carbon filter
HEPA filter
Fiber shield™ filter
Ultraviolet technology
Bipolar Ionization
DEVICE&APPLIANCE ACCESSORIES CERTIFICATION
EUROPEAN COMMUNITY CERTIFICATION
As defined by the Directive of EU LVD 2014/35/EUwith the following Standards IEC EN 60335
60417
BuildingService of
Hospitals.
49727/26-04-2010
Compliance based on specifications of the Ministry of Health
(Leak Integrity Test) / Hygiene Certificate (Hygiene Certificate) / Absolute
spreadsheets. Certificates and test report are delivered separately for each device
1822: 2019 Greek Regulations for the Hospital Building Service 49727 / 26
PaintAntibacterial activity
on plastic surfaces and other non
22196:2011-08, REPORT NO. 20.8.3.0016.
FilterAntibacterialactivity
PureAir Fiber Shield
TM
demonstrated its
Rhinovirus (host cell: MDCK) according to ISO 18184-2019 based on WP
approvals of EN and FDA, with antibacterial efficacy test compared with standards AATCC 100, AATCC147, JIS L1902, EN ISO 20645, ISO 18184. Us
standard, which controls the antiviral activity of any garment or woven material against viruses and
showed a reduction of pathogens by 96.5% after 30 minutes and 98.7% in 1 hour.
US FOOD & DRUG ADMINISTRATION
210(K) MEDICAL DEVICE CLEARANCES
HEPA FILTER CLASSIFICATION(S): EN1822 H14
resin binder.
WARRANTY TERMS
The guarantee is considered valid only in case of possession of the purchase document.
The warranty is waived for damages caused by failure to comply with the instructions
Failure to periodically inspect, maintain, repair or replace components due to
using products purchased or offered by our company. Damage caused by modification of device / system without
product, drop. Modifications or repairs by unauthorized personnel.
REFUNDS
To return defective materials, you must request the authorization to return goods by sending an email to the store that supplied
Only authorized products will be accepted, otherwise they will be rejected and
RESPONSIBILITY AND COMMITMENTS OF MANUFACTURER AND DISTRIBUTION COMPANY
The Company assumes no responsibility for any damage to individuals or property, due to failure to follow instructions or use
provided. We suggest you carefully read all the instructions or consult the Engineerin
upon request, circuit diagrams, lists of spare parts, instructions for calibrating lamps and other information, which are useful for repairing parts that t
considers serviceable. The company reserves the right to make changes without notice.
OPERATING
The filter and sterilization components of the device have the following time limits for proper operation and if you carry out the necessary supervision and maintenance of
the devices. The appliance must not be operated outdoors or in damp rooms, with a humidity of more than 70% or next to a humidifier, next to heaters, fireplaces or
appliances using gas. In environments with temperature fluctuations, as this can lead to water condensation inside. Under normal conditions,
SELF LIFE
4 - 5 years
1 - 2 years
1 - 2 years
1 - 2 years
13.000 operatinghours(required check annually)
4 - 5 years
CERTIFICATION
EUROPEAN COMMUNITY CERTIFICATION
As defined by the Directive of EU LVD 2014/35/EUwith the following Standards IEC EN 60335 -1 IEC EN 60335
Compliance based on specifications of the Ministry of Health
for E / M ΔΥ8 / Β /49727 / 26
(Leak Integrity Test) / Hygiene Certificate (Hygiene Certificate) / Absolute filter class (Filter category) /
spreadsheets. Certificates and test report are delivered separately for each device, with a unique production number. ISO 29463
1822: 2019 Greek Regulations for the Hospital Building Service 49727 / 26-04-2010.
on plastic surfaces and other non-porous surfaces for Staphylococcus aureus ATCC 6538P and Escherichia coli ATCC 8739 according to ISO
demonstrated its Antiviral ActivityRateof 96.58% for SARS-CoV-2, 98.13% for H1N1, 98.48% for H7N9, and 98.62% for
2019 based on WP-20096694-JC (01-04) test reports from a third party Independent Testing Laboratory. It carries the
and FDA, with antibacterial efficacy test compared with standards AATCC 100, AATCC147, JIS L1902, EN ISO 20645, ISO 18184. Us
standard, which controls the antiviral activity of any garment or woven material against viruses and
in particular tested against COVID
showed a reduction of pathogens by 96.5% after 30 minutes and 98.7% in 1 hour.
US FOOD & DRUG ADMINISTRATION
210(K) MEDICAL DEVICE CLEARANCES
US ENVIRONMENTAL PROTECTION
AGENCY ANTIMICROBIAL REGISTRATIONS
HEPA FILTER CLASSIFICATION(S): EN1822 H14
@ 2.5 cm/s Low resistance HEPA filter consisting of borosilicate microfiber with acrylic
The guarantee is considered valid only in case of possession of the purchase document.
failure to comply with the instructionsaccompanying the product at the time of purchase
pect, maintain, repair or replace components due to proper use.Use of incompatible spare parts or consumables. Compatibility is ensured only by
using products purchased or offered by our company. Damage caused by modification of device / system without prior consent of the company. Improper use of the
product, drop. Modifications or repairs by unauthorized personnel.
return defective materials, you must request the authorization to return goods by sending an email to the store that supplied
Only authorized products will be accepted, otherwise they will be rejected and returned to the sender.
ITMENTS OF MANUFACTURER AND DISTRIBUTION COMPANY
The Company assumes no responsibility for any damage to individuals or property, due to failure to follow instructions or use
provided. We suggest you carefully read all the instructions or consult the Engineering Department of our company. The manufacturer agrees with the buyer to provide,
, lists of spare parts, instructions for calibrating lamps and other information, which are useful for repairing parts that t
ders serviceable. The company reserves the right to make changes without notice.
t the necessary supervision and maintenance of
midity of more than 70% or next to a humidifier, next to heaters, fireplaces or
Under normal conditions,
filters need cleaning every
1 IEC EN 60335 -2 IEC EN 60529 IEC EN
/49727 / 26-04-2010 / Checking devices against leaks
filter class (Filter category) / Viruses Neutralization, with UVC power
with a unique production number. ISO 29463-2: 2018 / EN
nd Escherichia coli ATCC 8739 according to ISO
2, 98.13% for H1N1, 98.48% for H7N9, and 98.62% for
Independent Testing Laboratory. It carries the
and FDA, with antibacterial efficacy test compared with standards AATCC 100, AATCC147, JIS L1902, EN ISO 20645, ISO 18184. Using the ISO 18184
ar tested against COVID-19 (SARS-CoV-2)as filter materia
l
CLEARED FOR USE IN CLASS 1,2,3
MEDICAL DΕVICE FOR AIR FILTER
Low resistance HEPA filter consisting of borosilicate microfiber with acrylic
accompanying the product at the time of purchase:
Use of incompatible spare parts or consumables. Compatibility is ensured only by
prior consent of the company. Improper use of the
return defective materials, you must request the authorization to return goods by sending an email to the store that supplied the device or by calling its phone number.
ITMENTS OF MANUFACTURER AND DISTRIBUTION COMPANY
The Company assumes no responsibility for any damage to individuals or property, due to failure to follow instructions or use of technology without the safety provisions
g Department of our company. The manufacturer agrees with the buyer to provide,
, lists of spare parts, instructions for calibrating lamps and other information, which are useful for repairing parts that the manufacturer
