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EVS-EN 60601-2-39:2008/A11:2011

Elektrilised meditsiiniseadmed. Osa 2-39: Erinõuded kõhukelmedialüüsiseadmete esmasele ohutusele ja olulistele toimivusnäitajatele

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Kehtetu alates 03.06.2019
Alusdokumendid
EN 60601-2-39:2008/A11:2011
Tegevusala (ICS grupid)
11.040.99 Muud meditsiiniseadmed
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puuduvad

Standardi ajalugu

Staatus
Kuupäev
Tüüp
Nimetus
03.06.2019
Põhitekst
02.11.2011
Muudatus
09.01.2009
Põhitekst
This International Standard applies to the  BASIC SAFETY and  ESSENTIAL PERFORMANCE of PERITONEAL DIALYSIS ME EQUIPMENT as defined in 201.3.208, hereafter referred to as PD EQUIPMENT.  It applies to PD EQUIPMENT intended for use either by medical staff or under the supervision of medical experts, including PD EQUIPMENT operated by the PATIENT, regardless of whether the PD EQUIPMENT is used in a hospital or domestic environment. If a clause or subclause is specifically intended to be applicable to ME EQUIPMENT only, or to ME SYSTEMS only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to ME EQUIPMENT and to ME SYSTEMS, as relevant. HAZARDS inherent in the intended physiological function of ME EQUIPMENT or ME SYSTEMS within the scope of this standard are not covered by specific requirements in this standard except in 7.2.13 and 8.4.1 of the general standard. This standard can also be applied to  PD EQUIPMENT used for compensation or alleviation of disease, injury or disability. These particular requirements do not apply to the  DIALYSING SOLUTION, or the  DIALYSING SOLUTION CIRCUIT.

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