Askle Sante WINNCARE automorpho AUTOMORPHO XL Gebruikershandleiding - Pagina 6

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E

INDICATIONS

In the opinion of the Committee for Evaluation of Goods and Services published in the Journal Officiel on 21 July 2005 and in the
opinion of clinical experts:
Prevention and aid to treatment of eschars from stages 1 to 4 (according to medical opinion) in patients confined to bed for more
than 15 hours, presenting with a risk of eschars assessed against a validated scale and clinical judgment.
Patients whose weight cannot be determined.
F

PRECAUTIONS

Non-stabilised and/or muscular trauma in contact with the support;
Days immediately following surgical intervention on eschar (skin graft or pedicled graft) [ prefer static mode];
Patient monitored at home without the possibility of intervention by medical auxiliaries;
The device must not be used in a hyperbaric chamber.
WARNING:
According to appendix 1 to European Directive 93/42/CEE relating to the essential criteria applicable to medical devices, only
compatibility between systems assembled by the manufacturer, ASKLESANTE, guarantees a safe combination when using the
AXTAIR motorised air mattress.
The specification and performance of the motorised air support will only be maintained by using the AXTAIR pump [ref.
VAXT4/POMPE/AUTO], associated with the AXTAIR mattress [ref. VAXT4/MA/AUTO or VAXT4/MA/XL] and, optionally, the
inflation/deflation kit [ref. VKIT/AXT].
The national authority responsible for health and safety and health products can at any time institute audits of the conditions under
which said products are marketed and take the measures necessary if there is danger or a breach of the rules. In the event of failure
to comply with the abovementioned conditions of use, the user's liability may be committed if there is an accident.
PLEASE NOTE: The compressor and the mattress are still compatible with the products with equivalent
references from previous ranges
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