Clinical Research Directory

Inclusion Criteria 1. Able and willing to provide informed consent and to complete a follow-up visit at 14 ± 7 days post-procedure. 2. Individuals undergoing catheter-based procedures utilizing 6F to 12F inner diameter procedural sheaths, with single or multiple venous access sites in one or both limbs. 3. Individuals who are candidates to have their venous access site(s) closed with MYNX CONTROL™ VENOUS VCD 6F-12F per IFU. 4. At the time of enrollment, the Investigator deems the subject a candidate for same-day discharge (SDD) per standard of care (no procedure related events/complications e.g., no new pericardial effusion, post-procedure diuresis not needed, etc.). Exclusion Criteria 1. Presence of bruit, palpable aneurysm, significant candida or groin infection. 2. Prior to closure, presence of hematoma in the accessed limb. 3. Currently involved in any other clinical trial that may interfere with the outcomes of this study as determined by the Investigator. 4. Planned use of other closure devices or techniques other than MYNX CONTROL™ VENOUS VCD 6F-12F. 5. Life expectancy \<12 months.