Number of the records: 1
schválenie zdravotníckeho vybavenia
Record number d018795 Date 06.06.2025 Type M - MESH Topical term schválenie zdravotníckeho vybavenia Other term English (Pseudonym) Device Approval Process
English (Pseudonym) New Device Approval
Slovak (Pseudonym) registrácia zdravotníckych pomôcok
UDC E05.337.275N06.850.210.275 Note Process that is gone through in order for a device to receive approval by a government regulatory agency. This includes any required preclinical or clinical testing, review, submission, and evaluation of the applications and test results, and post-marketing surveillance. It is not restricted to FDA. 
subject heading
Number of the records: 1