Примери за използване на Diagnostic medical на Английски и техните преводи на Български
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in vitro diagnostic medical devices imported from outside the EU?
(2009) Children's exposure to diagnostic medical radiation and cancer risk:
In this connection, the manufacturer shall inform the notified body whether any such change is likely to affect the performance of the in vitro diagnostic medical device concerned. 5.
Students who have successfully completed the Bachelor of Science degree program qualify for the American Registry for Diagnostic Medical Sonography(ARDMS) national board examination
A separate law will also ensure that the new rules also apply to in vitro diagnostic medical devices, i.e.
The Diagnostic Medical Sonography program is accredited from the Joint Review Committee on Education in Diagnostic Medical Sonography.
clinical training in the field of general diagnostic medical sonography(ultrasound).
Sonographers, also known as Ultrasound Technologists, or Diagnostic Medical Sonographers, use advanced imaging procedures.
Directive 98/79/EC of the European Parliament and of the Council on diagnostic medical devices in vitro.
In this connection, the manufacturer shall inform the notified body whether any such change is likely to affect the performance of the in vitro diagnostic medical device concerned.
in vitro diagnostic medical devices.
in vitro diagnostic medical devices back to their supplier.
Devices intended for performance evaluation referred to in the Directive on in vitro diagnostic medical devices;
of the Council on in vitro diagnostic medical devices.
dental hygienist courses and diagnostic medical sonography.
essentially for the purpose of the conformity assessment procedures, to group in vitro diagnostic medical devices into two main product classes;
Whereas the list of in vitro diagnostic medical devices to be subjected to third-party conformity assessment needs updating,
free movement of the in vitro diagnostic medical devices to which it applies;
Products for general laboratory use are not in vitro diagnostic medical devices unless such products,
should be replaced by a single legislative act applicable to all medical devices other than in vitro diagnostic medical devices.