EU Medical Device Labeling Regulation and the Unintended Consequence on Sterilized Product, the Environment, and the Health and Safety of People

Biomed Instrum Technol. 2020 Jun 1;54(s1):84-88. doi: 10.2345/0899-8205-54.s3.84.
No abstract available

MeSH terms

  • Device Approval*
  • Humans
  • Medical Device Legislation*
  • Product Labeling