Introduction The lack of a terminology to compare medical devices together with the arbitrary and opaque nature of product registration systems are major obstacles to a more informed decision process regarding the use and acquisition of new medical devices. This paper describes the systematization of information to help in the identification of similar cardiovascular implantable devices. Methods The systematization was developed in four stages: definition of the technical attributes of each device group; classification of a sample of devices; implementation of the proposed systematization in Protégé; and evaluation of the application. The systematization dealt with a set of common attributes – indication of use, anatomic location, manufact...
MONITORINGTHESAFETYOFapproved medical prod-uctsisofvitalpublichealthimportance, given that in clinic...
This document represents expert consensus concerning the Monitoring of Cardiovascular Implantable El...
Medical device manufacturers must continuously evaluate all clinical data available for their produc...
Introduction The lack of a terminology to compare medical devices together with the arbitrary and op...
International audienceThe patient population benefitting from cardiac implantable electronic devices...
A medical device identifier can identify an implanted medical device. In one example arrangement, th...
Objective: To describe the features of computer program to support the activity of the responsible f...
Cardiovascular implantable electronic devices (CIEDs) have expanded in number and complexity since t...
textabstractRecent safety issues involving non-active implantable medical devices (NAIMDs) have high...
In the Dutch Arthroplasty Register (LROI), the product and batch number of prosthetic components and...
Inventory is a fundamental process throughout the life cycle of medical devices. The maintenance pro...
Medical devices are found in modern hospitals, medical practices and laboratories. These specialized...
Implantable Electronic Medical Devices provides a thorough review of the application of implantable ...
□ In the Dutch Arthroplasty Register (LROI), the product and batch number of prosthetic components a...
Background—Postmarket medical device surveillance in the United States depends largely on voluntary ...
MONITORINGTHESAFETYOFapproved medical prod-uctsisofvitalpublichealthimportance, given that in clinic...
This document represents expert consensus concerning the Monitoring of Cardiovascular Implantable El...
Medical device manufacturers must continuously evaluate all clinical data available for their produc...
Introduction The lack of a terminology to compare medical devices together with the arbitrary and op...
International audienceThe patient population benefitting from cardiac implantable electronic devices...
A medical device identifier can identify an implanted medical device. In one example arrangement, th...
Objective: To describe the features of computer program to support the activity of the responsible f...
Cardiovascular implantable electronic devices (CIEDs) have expanded in number and complexity since t...
textabstractRecent safety issues involving non-active implantable medical devices (NAIMDs) have high...
In the Dutch Arthroplasty Register (LROI), the product and batch number of prosthetic components and...
Inventory is a fundamental process throughout the life cycle of medical devices. The maintenance pro...
Medical devices are found in modern hospitals, medical practices and laboratories. These specialized...
Implantable Electronic Medical Devices provides a thorough review of the application of implantable ...
□ In the Dutch Arthroplasty Register (LROI), the product and batch number of prosthetic components a...
Background—Postmarket medical device surveillance in the United States depends largely on voluntary ...
MONITORINGTHESAFETYOFapproved medical prod-uctsisofvitalpublichealthimportance, given that in clinic...
This document represents expert consensus concerning the Monitoring of Cardiovascular Implantable El...
Medical device manufacturers must continuously evaluate all clinical data available for their produc...