Lowenstein Medical Allegra M30 Mode D'emploi page 42

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The safety of the secretion aspirator Allegra M30 complies with the
acknowledged rules of technology and meets the requirements of the
German Medical Devices Act.
The secretion aspirator Allegra M30 bears the CE marking
EN
CE0044 in accordance with the EU Council Directive 93/42/EEC concern-
ing medical devices and meets the essential requirements of Annex I of this
directive.
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The secretion aspirator Allegra M30 has been tested in accordance
with IEC 62353.
The quality management system applied by
Löwenstein Medical GmbH & Co. KG is certified in compliance with the rele-
vant international standards.
The secretion aspirator Allegra M30 is a medical aspirator classified as
class lla in accordance with EU Council Directive 93/42/EEC, Annex IX.
Errors and omissions excepted.