Medical device (MD) nomenclatures are essential for market surveillance and vigilance activities. Currently, more than 25 arthroplasty Registries are established in Europe, each of them based on a different MD nomenclature. A common and shared nomenclature of orthopaedic implants is important to analyse implant performance across different national databases referring to a unique definition of its characteristics. Aim of this study is to describe an approach to compare and harmonise two different nomenclatures: a first step towards the organization of an international nomenclature of medical devices
With the implementation of the new MDR 2017/745 by the European Parliament, more robust clinical and...
Abstract Background The serious adverse events associated with metal on metal hip replacements have ...
The Poly Implant Prothèse (PIP) scandal in France prompted a revision of the regulations regarding t...
There are many purposes for using a nomenclature of medical devices. The Italian CND is a free publi...
AbstractInventory is a fundamental process throughout the life cycle of medical devices. The mainten...
□ In the Dutch Arthroplasty Register (LROI), the product and batch number of prosthetic components a...
Medical devices have different nomenclatures for their classification. Some of the most significant ...
In the Dutch Arthroplasty Register (LROI), the product and batch number of prosthetic components and...
Background: The European Union Medical Device Regulation (MDR) requires manufacturers to undertake p...
International audienceSurveillance and traceability of medical devices (MD) is a challenge in health...
Innovations in Orthopaedics and Traumatology have contributed to the achievement of a high-quality l...
The general shortage of evidence regarding benefits and harms of medical devices has been highlighte...
Accurate prosthesis classification is critical for total joint arthroplasty surveillance and assessm...
Medical device manufacturers must continuously evaluate all clinical data available for their produc...
With the implementation of the new MDR 2017/745 by the European Parliament, more robust clinical and...
Abstract Background The serious adverse events associated with metal on metal hip replacements have ...
The Poly Implant Prothèse (PIP) scandal in France prompted a revision of the regulations regarding t...
There are many purposes for using a nomenclature of medical devices. The Italian CND is a free publi...
AbstractInventory is a fundamental process throughout the life cycle of medical devices. The mainten...
□ In the Dutch Arthroplasty Register (LROI), the product and batch number of prosthetic components a...
Medical devices have different nomenclatures for their classification. Some of the most significant ...
In the Dutch Arthroplasty Register (LROI), the product and batch number of prosthetic components and...
Background: The European Union Medical Device Regulation (MDR) requires manufacturers to undertake p...
International audienceSurveillance and traceability of medical devices (MD) is a challenge in health...
Innovations in Orthopaedics and Traumatology have contributed to the achievement of a high-quality l...
The general shortage of evidence regarding benefits and harms of medical devices has been highlighte...
Accurate prosthesis classification is critical for total joint arthroplasty surveillance and assessm...
Medical device manufacturers must continuously evaluate all clinical data available for their produc...
With the implementation of the new MDR 2017/745 by the European Parliament, more robust clinical and...
Abstract Background The serious adverse events associated with metal on metal hip replacements have ...
The Poly Implant Prothèse (PIP) scandal in France prompted a revision of the regulations regarding t...