Adept Medical MR Safe AM4000 Manuel d'utilisation - Page 8
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Approved Cleaners List
Approved Disinfectant by Brands
Liquids:
Dissolvable:
ORION Laboratories
Du Pont
70% Isopropyl Alcohol
Rely+On Virkon Tablets
Jaychem Industries
2% Chlorhexidine / 70% Alcohol
Betadine
Povidone Iodine (7.5%)
BODE Chemie GmbH
Kohrsolin FF
STERIS
Coverage Spray TB
CaviCide
Metrex Research
Approved Active Disinfectant Ingredients
Acid Based:
≤10% Malic Acid CAS 6915-15-7
≤6% Sulfamic acid CAS 5329-14-6
Alcohol Based:
≤5% 2-Butoxyethanol CAS 111-76-2
≤10% Butyldiglycol CAS 112-34-5
≤70% Isopropyl Alcohol (Propan-2-ol) CAS 67-63-0
≤10% Tridecanol CAS 69011-36-5
<10% Alcohols, C12-14, ethoxylated CAS 68439-50-9
Sulphate Based:
≤0.1% PHMB CAS 27083-27-8
≤55% Potassium Peroxymonosulfate CAS 70693-62-8
≤3% Potassium Persulfate CAS 7727-21-1
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Surface Wipes:
PDI Sani-Cloth Bleach
PDI Sani-Cloth AF3
Reynard Health Supplies
Surface Disinfectant Wipes
Metrex Research
CaviWipes
Clinell Wipes
Ammonium and Chloride Based:
≤5% Benzalkonium Chloride CAS 68424-85-1
≤0.28% Benzethonium Chloride CAS 121-54-0
≤10% Benzyl-C23-18-Alkyl-dimethyl Ammonium Chloride
CAS 8001-54-5
≤2% Chlorhexidine CAS 55-56-1
≤10% Didecyl Dimethyl Ammonium chloride CAS 7173-51-5
≤0.5% Quaternary Ammonium Compounds CAS
68956-79-6
<5% Benzyl-C 12-18 alkyldimethylammonium chlorides
CAS 63891-01-5
Others:
≤10% Glutaral CAS 111-30-8
≤0.63% Sodium Hypochlorite CAS 7681-52-9
≤7.5% Povidone Iodine CAS 25655-41-8
0.5% Disodium Cocoampho Dipropionate CAS68604-71-7
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Drying
All components should be dried thoroughly
before use.
Maintenance, Inspection and Testing
For all components ensure:
●
No visible damage or sharp edges, e.g.
cracks.
Locking Leg Assembly:
●
Ensure blue lever functions smoothly.
●
Ensure when lever is in the unlocked
position the Locking Leg Assembly can
extend and contract smoothly when force
is applied.
●
Ensure when lever is in the locked
position the Locking Leg Assembly
cannot contract or extend when force is
applied.
●
Ensure smooth engagement with
daggerboard during assembly.
●
Ensure tight fit with Armrest Wing during
assembly.
Packaging
It is not required to package the device following
disinfection.
Sterilisation
This device should not be subjected to
sterilisation processes.
Storage
Once disinfection is complete and all
components are dry the device should be stored
in a dry environment.
!
The instructions provided above have been validated
by the manufacturer of the medical device as being
capable of preparing a medical device for reuse. It
remains the responsibility of the processor to ensure
that the processing, as actually performed using
equipment, materials and personnel in the processing
facility, achieves the desired result. This requires
verification and/or validation and routine monitoring
of the process.
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Disposal
Used product is a biohazard, decontaminate
according to instruction provided in the
Disinfection Instructions and reach out to the
manufacturer on [email protected]
for material specification, if required. Dispose
according to internal clinic policy taking into
consideration local regulations.
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