دورية أكاديمية
Availability of Unique Device Identifiers for Class I Medical Device Recalls From 2018 to 2022.
| العنوان: | Availability of Unique Device Identifiers for Class I Medical Device Recalls From 2018 to 2022. |
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| المؤلفون: | Mooghali M; Section of General Internal Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, Connecticut.; Yale Collaboration for Regulatory Rigor, Integrity, and Transparency, Yale School of Medicine, New Haven, Connecticut., Ross JS; Section of General Internal Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, Connecticut.; Yale Collaboration for Regulatory Rigor, Integrity, and Transparency, Yale School of Medicine, New Haven, Connecticut.; Center for Outcomes Research and Evaluation, Department of Health Policy and Management, Yale School of Public Health, Yale-New Haven Health System, New Haven, Connecticut., Kadakia KT; Harvard Medical School, Boston, Massachusetts., Dhruva SS; Section of Cardiology, Department of Medicine, University of California San Francisco School of Medicine, San Francisco.; San Francisco Veterans Affairs Health Care System, San Francisco, California. |
| المصدر: | JAMA internal medicine [JAMA Intern Med] 2023 Jul 01; Vol. 183 (7), pp. 735-737. |
| نوع المنشور: | Journal Article; Research Support, U.S. Gov't, P.H.S. |
| اللغة: | English |
| بيانات الدورية: | Publisher: American Medical Association Country of Publication: United States NLM ID: 101589534 Publication Model: Print Cited Medium: Internet ISSN: 2168-6114 (Electronic) Linking ISSN: 21686106 NLM ISO Abbreviation: JAMA Intern Med Subsets: MEDLINE |
| أسماء مطبوعة: | Original Publication: Chicago, IL : American Medical Association, [2013]- |
| مواضيع طبية MeSH: | Medical Device Recalls* , Device Approval*, Humans ; United States ; Risk Factors ; United States Food and Drug Administration ; Product Surveillance, Postmarketing |
| معلومات مُعتمدة: | U01 FD005938 United States FD FDA HHS; UL1 TR001863 United States TR NCATS NIH HHS |
| فهرسة مساهمة: | Local Abstract: [plain-language-summary] This cross-sectional study describes the inclusion of unique device identifier in recall notices for moderate- and high-risk medical devices in the US. |
| تواريخ الأحداث: | Date Created: 20230515 Date Completed: 20230705 Latest Revision: 20240516 |
| رمز التحديث: | 20240516 |
| مُعرف محوري في PubMed: | PMC10186206 |
| DOI: | 10.1001/jamainternmed.2023.0727 |
| PMID: | 37184854 |
| قاعدة البيانات: | MEDLINE |
| تدمد: | 2168-6114 |
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| DOI: | 10.1001/jamainternmed.2023.0727 |