Home / Dz.U. 2011 nr 16 poz. 75
Regulation of the Minister of Health of January 12, 2011, on the essential requirements and conformity assessment procedures for in vitro diagnostic medical devices
Rozporządzenie Ministra Zdrowia z dnia 12 stycznia 2011 r. w sprawie wymagań zasadniczych oraz procedur oceny zgodności wyrobów medycznych do diagnostyki in vitro
Type
Regulation (Rozporządzenie)
Status
act has a consolidated text (akt posiada tekst jednolity)
Announced
2011-01-12
Entry into force
2011-01-24
Texts
Keywords
Medical Productsbezpieczeństwo produktów
Related acts
Amending Acts (1)
Information on Consolidated Text (1)
Legal Basis (1)
Legal Basis from Art. (1)
- Law of May 20, 2010 on medical devices · art. 23 ust. 3
Repeals Resulting From (1)
- Law of April 7, 2022, on medical devices · 2040-05-26
Acts referring to this act
- Acts Declared Repealed: Law of April 7, 2022, on medical devices
- Implementing Regulations: Law of May 20, 2010 on medical devices
- Amended Acts: Regulation of the Minister of Health of April 10, 2012, amending the regulation on essential requirements and conformity assessment procedures for in vitro diagnostic medical devices
- Consolidated Text for an Act: Announcement of the Minister of Health of June 6, 2013, on the promulgation of the consolidated text of the Regulation of the Minister of Health on the essential requirements and conformity assessment procedures for in vitro diagnostic medical devices