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Availability of Unique Device Identifiers for Class I Medical Device Recalls From 2018 to 2022.
Mooghali, Maryam; Ross, Joseph S; Kadakia, Kushal T; Dhruva, Sanket S.
Affiliation
  • Mooghali M; Section of General Internal Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, Connecticut.
  • Ross JS; Yale Collaboration for Regulatory Rigor, Integrity, and Transparency, Yale School of Medicine, New Haven, Connecticut.
  • Kadakia KT; Section of General Internal Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, Connecticut.
  • Dhruva SS; Yale Collaboration for Regulatory Rigor, Integrity, and Transparency, Yale School of Medicine, New Haven, Connecticut.
JAMA Intern Med ; 183(7): 735-737, 2023 07 01.
Article in En | MEDLINE | ID: mdl-37184854
This cross-sectional study describes the inclusion of unique device identifier in recall notices for moderate- and high-risk medical devices in the US.
Subject(s)
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Device Approval / Medical Device Recalls Type of study: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Country/Region as subject: America do norte Language: En Journal: JAMA Intern Med Year: 2023 Document type: Article
Fulltext
Add to My VHL
Print
XML
PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Device Approval / Medical Device Recalls Type of study: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Country/Region as subject: America do norte Language: En Journal: JAMA Intern Med Year: 2023 Document type: Article