Lowenstein Medical Allegra M30 Mode D'emploi page 50

The safety of the secretion aspirator Allegra M30 complies with the ac-
knowledged rules of technology and meets the requirements of the
German Medical Devices Act.
The secretion aspirator Allegra M30 bears the CE marking CE0197 in
accordance with the EU Council Directive 93/42/EEC concerning medical devices
and meets the essential requirements of Annex I of this directive.
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 relevant
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.
EN
Errors and omissions excepted.
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