Read the untranslated law here: http://www.ris.bka.gv.at/Dokumente/BgblAuth/BGBLA_2013_II_268/BGBLA_2013_II_268.html
268. Regulation of the Federal Minister for health, with the accompanying measures to the Regulation (EU) No. 722/2012 be taken (MPTG-VO)
On the basis of § 77 para 3 of the medical devices act, Federal Law Gazette No. 657/1996, as last amended by the Federal Act Federal Law Gazette I no. 143/2009, is prescribed:
§ 1 (1) the enforcement of Regulation (EU) No. 722/2012 on specific requirements regarding the requirements laid down in Directive 90/385/EEC or Council Directive 93/42/EEC to using of tissue of animal origin produced active implantable medical devices and medical devices, OJ No. L 212 of the 9.8.2012, p. 3, is in accordance with the paragraph 2 the Federal Office for security in healthcare.
(2) article 4 of Regulation (EU) lie in whether no. 722 / 2012-controlled tasks the Federal Ministers responsible for the matters of health care.
2. (1) this regulation with 29 August 2013 enter into force.
(2) with the entry into force of this regulation, the regulation of the Federal Minister for health and women regarding requirements for medical products of 93/42/EEC enters, produced using tissues of animal origin (MTGV), Federal Law Gazette II No. 579/2003, override.
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