+ Site Statistics
References:
54,258,434
Abstracts:
29,560,870
PMIDs:
28,072,757
+ Search Articles
+ PDF Full Text Service
How our service works
Request PDF Full Text
+ Follow Us
Follow on Facebook
Follow on Twitter
Follow on LinkedIn
+ Subscribe to Site Feeds
Most Shared
PDF Full Text
+ Translate
+ Recently Requested

New FDA medical device rule imposes minimal burden on hospitals: facilities able to scan unique device identifiers will benefit



New FDA medical device rule imposes minimal burden on hospitals: facilities able to scan unique device identifiers will benefit



P and T 38(12): 720



New FDA rules on medical devices shouldn't be a burden for hospitals that can scan unique device identifiers.

Please choose payment method:






(PDF emailed within 1 workday: $29.90)

Accession: 054596959

Download citation: RISBibTeXText

PMID: 24391393


Related references

Unique device identifiers for coronary stent postmarket surveillance and research: a report from the Food and Drug Administration Medical Device Epidemiology Network Unique Device Identifier demonstration. American Heart Journal 168(4): 405-413.E2, 2015

The Safe Medical Devices Act of 1989: a burden on medical facilities, device manufacturers, and the FDA?. Biomedical Instrumentation and Technology 24(2): 79-83, 1990

The Value of Unique Device Identifiers in Plastic Surgery. Aesthetic Surgery Journal 38(11): 1264-1266, 2018

Fulfilling the Promise of Unique Device Identifiers. Annals of Internal Medicine 169(3): 183-185, 2018

Medical devices--establishment of procedures to make a device a banned device: final rule. Federal Register 44(98): 29213-29224, 1979

Medical devices: classification of the dental sonography device and jaw tracking device. Final rule. Federal Register 68(231): 67365-7, 2003

Constructing the informatics and information technology foundations of a medical device evaluation system: a report from the FDA unique device identifier demonstration. Journal of the American Medical Informatics Association, 2017

Mutual recognition of pharmaceutical good manufacturing practice inspection reports, medical device quality system audit reports, and certain medical device product evaluation reports between the United States and the European Community--FDA. Final rule. Federal Register 63(215): 60122-60164, 1998

Nicht belegter oder erwartbarer Benefit durch neues Device in der Shuntchirurgie; Not confirmed or expectable benefit of a new device in shunt surgery;. Gefässchirurgie 24(4): 341-343, 2019

Mutual Recognition of the Food and Drug Administration and European Community Member State Conformity Assessment Procedures; pharmaceutical GMP inspection reports, medical device quality system evaluation reports, and certain medical device premarket evaluation reports--FDA. Proposed rule. Federal Register 63(69): 17744-17771, 1998

Hospitals whacked by RAC. The audit program imposes a crushing burden on hospitals. Can it be fixed?. Trustee 67(3): 15-6, 23-4, 1, 2014

Unique device identification system. Final rule. Federal Register 78(185): 58785-58828, 2013

FDA issues Unique Device Identification final rule. Or Manager 29(11): 5, 26, 2014

New device GMPs benefit hospitals. Purchasing Administration 2(9): 7-7, 1978

A roundtable discussion: hopes and hurdles for the unique device identification rule. Biomedical Instrumentation and Technology 49(3): 188-194, 2015