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Start Over Subjects Equipment Safety ✖Remove constraint Subjects: Equipment Safety

11. Emergency use authorization of medical products and related authorities: guidance for industry and other stakeholders

Publication:
Silver Spring, MD : Food and Drug Administration, U.S. Department of Health and Human Services, January 2017
Subject(s):
Civil Defense -- legislation & jurisprudence
Device Approval
Drug Approval
Emergencies
Terrorism
Emergency Medical Services
Equipment Safety
Off-Label Use
Public Health
Safety
Humans
United States
United States. Department of Health and Human Services.
United States. Department of Homeland Security.
United States. Food and Drug Administration.

12. Use of real-world evidence to support regulatory decision-making for medical devices: guidance for industry and Food and Drug Administration staff

Publication:
Silver Spring, MD : Center for Devices and Radiological Health, August 31, 2017
Subject(s):
Equipment and Supplies
Equipment Safety
Evidence-Based Medicine
Product Surveillance, Postmarketing
Data Collection
Data Interpretation, Statistical
Decision Making
Device Approval
Quality Control
Humans
United States
United States. Department of Health and Human Services.
United States. Food and Drug Administration.

13. Establishing the performance characteristics of in vitro diagnostic devices for the detection or detection and differentiation of human papillomaviruses: guidance for Industry and Food and Drug Administration staff

Publication:
Silver Spring, MD : Center for Devices and Radiological Health, September 15, 2017
Subject(s):
Device Approval
Papillomavirus Infections -- diagnosis
Reagent Kits, Diagnostic -- standards
Cervix Uteri -- cytology
Cervix Uteri -- virology
Equipment Failure
Equipment Safety
Genotyping Techniques -- standards
Mass Screening
Papillomaviridae -- classification
Papillomaviridae -- genetics
Quality Control
Reference Standards
Reproducibility of Results
Research Design
Specimen Handling
Humans
United States
United States. Department of Health and Human Services.
United States. Food and Drug Administration.

14. Data Snapshot: dislodged tubes and lines

Author(s):
Feil, Michelle, author
Publication:
[Harrisburg, Pa.] : Pennsylvania Patient Safety Authority, September 2017
Subject(s):
Catheterization -- adverse effects
Catheterization -- mortality
Catheters -- adverse effects
Equipment Failure
Equipment Safety
Intubation -- adverse effects
Intubation -- instrumentation
Intubation -- mortality
Catheterization, Peripheral -- adverse effects
Catheterization, Peripheral -- instrumentation
Catheterization, Peripheral -- mortality
Catheters, Indwelling -- adverse effects
Drainage -- adverse effects
Drainage -- instrumentation
Drainage -- mortality
Intubation, Gastrointestinal -- adverse effects
Intubation, Gastrointestinal -- instrumentation
Intubation, Gastrointestinal -- mortality
Patient safety
Humans
Pennsylvania
United States

18. CT contrast media power injectors can rupture conventional IV sets

Publication:
[Harrisburg, Pa.] : Pennsylvania Patient Safety Authority, c2008
Subject(s):
Contrast Media
Cross Infection -- prevention & control
Equipment Failure
Injections, Intravenous -- instrumentation
Tomography, X-Ray Computed -- instrumentation
Equipment Safety
Guidelines as Topic
Pressure
Humans
Pennsylvania
United States
United States. Food and Drug Administration.

20. Tubing misconnections: making the connection to patient safety

Publication:
[Harrisburg, Pa.] : Pennsylvania Patient Safety Authority, c2010
Subject(s):
Equipment Design -- adverse effects
Equipment Safety
Medical Errors -- prevention & control
Safety Management -- methods
Catheterization -- adverse effects
Catheterization -- instrumentation
Drug Delivery Systems -- instrumentation
Enteral Nutrition -- adverse effects
Enteral Nutrition -- instrumentation
Equipment and Supplies, Hospital
Infusions, Intravenous -- adverse effects
Infusions, Intravenous -- instrumentation
Intubation -- adverse effects
Intubation -- instrumentation
Materials Management, Hospital
Humans
United States