Technical considerations for additive manufactured medical devices: guidance for industry and Food and Drug Administration staff
- Collection:
- Health Policy and Services Research
- Series Title(s):
- Guidance for industry
- Contributor(s):
- United States. Department of Health and Human Services, issuing body. United States. Food and Drug Administration, issuing body. Center for Biologics Evaluation and Research (U.S.), issuing body. Center for Devices and Radiological Health (U.S.), issuing body.
- Publication:
- Silver Spring, MD : Center for Biologics Evaluation and Research, December 5, 2017
- Language(s):
- English
- Format:
- Text
- Subject(s):
- Computer-Aided Design -- standards Device Approval Manufactured Materials -- standards Materials Testing -- standards Printing, Three-Dimensional -- standards Quality Control Computer Security -- standards Diagnostic Imaging Models, Anatomic Product Labeling -- standards Reproducibility of Results Software -- standards Sterilization -- standards Humans United States United States. Department of Health and Human Services. United States. Food and Drug Administration.
- Genre(s):
- Guideline Technical Report
- Copyright:
- The National Library of Medicine believes this item to be in the public domain. (More information)
- Extent:
- 1 online resource (1 PDF file (28 pages)).
- NLM Unique ID:
- 101720001 (See catalog record)
- Permanent Link:
- http://resource.nlm.nih.gov/101720001