Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Third-party reprocessing of endoscopic accessories.

P J Furman1

  • 1Association of Medical Device Reprocessors, Washington, DC 20036, USA.

Gastrointestinal Endoscopy Clinics of North America
|February 22, 2000
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Single-use device reprocessing.

FDA consumer·2001
Same author

Electrodepolarization of the facial nerve for hemifacial spasm: experimental studies.

Surgical forum·1968
Same journal

Transform-The Path Forward: Endoscopy and the Science of Expertise.

Gastrointestinal endoscopy clinics of North America·2026
Same journal

Ushering in a New Era of Training in Endoscopy.

Gastrointestinal endoscopy clinics of North America·2026
Same journal

Where Do We Go from Here: Transforming Teaching Endoscopy Knowledge Using the Expert Performance Approach.

Gastrointestinal endoscopy clinics of North America·2026
Same journal

Integrating Artificial Intelligence into Endoscopy Training.

Gastrointestinal endoscopy clinics of North America·2026
Same journal

From Expert to Educator: Translating Expert Performance into Teachable Competencies Through Trainer Development in Endoscopic Simulation.

Gastrointestinal endoscopy clinics of North America·2026
Same journal

Implementing Endoscopy Simulation Nationally.

Gastrointestinal endoscopy clinics of North America·2026
See all related articles

Third-party reprocessing of single-use medical devices is safe and FDA-regulated, reducing hospital costs without impacting patient safety. Manufacturers

Area of Science:

  • Medical device regulation
  • Healthcare economics
  • Patient safety

Background:

  • Third-party reprocessing of medical devices labeled for single use is a safe, FDA-regulated practice.
  • This practice assists hospitals in reducing costs while maintaining patient care standards.
  • The designation of a device as 'single use' by manufacturers is not always based on clinical necessity but can be influenced by economic factors, as clear FDA standards differentiating reusable from single-use devices are lacking.

Purpose of the Study:

  • To evaluate the safety and regulatory status of third-party reprocessing for single-use medical devices.
  • To highlight the economic benefits of reprocessing for healthcare institutions.
  • To discuss the current regulatory framework and its ongoing review by the FDA.

Main Methods:

Related Experiment Videos

  • Analysis of the existing FDA regulatory framework for medical device reprocessing.
  • Review of quality assurance requirements for third-party reprocessors.
  • Examination of the criteria used by manufacturers to label devices as single-use.

Main Results:

  • Third-party reprocessing is confirmed as a safe and FDA-regulated practice.
  • Reprocessing offers significant cost-saving opportunities for hospitals.
  • The FDA is currently reviewing and developing a new regulatory scheme for device reprocessing.

Conclusions:

  • Third-party reprocessing of single-use medical devices is a viable and safe option.
  • The practice contributes to healthcare cost reduction without compromising patient safety.
  • The evolving FDA regulations aim to further standardize and ensure the safety of medical device reprocessing.