Analytical methods for the determination of DEHP plasticizer alternatives present in medical devices: A review

Author:

Bernard L.,Décaudin B.,Lecoeur M.,Richard D.,Bourdeaux D.,Cueff R.,Sautou V.

Funder

French Medicine Agency (Grant no. AAPR-2012-9) (ANSM: Agence Nationale de Sécurité des Médicaments et des Produits de Santé)

Publisher

Elsevier BV

Subject

Analytical Chemistry

Reference109 articles.

1. PVCMed Alliance – PVC Healthcare Applications, accessed 〈http://www.pvcmed.org/learning-centre/pvc-medical-applications/〉.

2. Center for Devices and Radiological Health, U.S. Food and Drug Administration, Safety Assessment of Di(2-ethylhexyl)phthalate (DEHP) Released from PVC Medical Devices, U.S Food and Drug Administration (FDA), Rockville, 2002, accessed 〈http://www.fda.gov/downloads/medicaldevices/deviceregulationandguidance/guidancedocuments/ucm080457.pdf〉.

3. Phthalates: Toxicology and exposure

4. European Union, Regulation (EC) No. 1272/2008 of the European Parliament and of the Council on Classification, Labelling and Packaging of Substances and Mixtures, Amending and Repealing Directives 67/548/EEC and 1999/45/EC, and Amending Regulation (EC) No. 1907/2006, 2008.

5. European Union, Directive 2007/47/EC of The European Parliament and of the Council of 5 September 2007 Amending Council Directive 90/385/EEC on the Approximation of the Laws of the Member States Relating to Active Implantable Medical Devices, Council Directive 93/42/EEC Concerning Medical Devices and Directive 98/8/EC Concerning the Placing of Biocidal Products on the Market.

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