A Clinical Registry to Demonstrate the Safety and Performance of Teleflex Vascular Access Devices

The objective of Teleflex's Vascular Access Device Registry (VADER) is to provide high-quality data on the performance, safety, and clinical benefits of Teleflex's vascular access devices when used in a real-world setting

Inclusion Criteria: * Subjects will undergo a procedure that will include use of a Teleflex device covered by this Research. * Subject is willing and capable of providing informed consent and/or give approval to collect, store and process limited health information by the Sponsor; or such consent is provided by a legally designated representative if required by local law or regulation. * Subjects is able to read and understand English or Spanish languages Exclusion Criteria: * Subject is currently participating in another clinical Registry or investigation that may confound the results of this Registry. * Subject was previously failed screening or was enrolled in this clinical Registry. * Subject is imprisoned * Subject is cognitively impaired and unable to provide informed consent