+Article 33 1

Article 33 1

1.   Before making an EHR system available on the market, distributors shall verify that:

(a)

the manufacturer has drawn up the EU declaration of conformity;

(b)

the EHR system bears the CE marking of conformity;

(c)

the EHR system is accompanied by the information sheet referred to in Article 38 with clear and complete instructions for use in accessible formats;

(d)

where applicable, the importer has complied with the requirements set out in Article 32(3).

1. Prehľad

,

1.1 Odkazy

1.2 Identifikované požiadavky

1.3 Súvisiace štandardy

2. Identifikované požiadavky

Požiadavky

3. Súvisiace štandardy

Štandardy