
Coloplast A/S
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CONVEEN INTERMITTENT CATHETERS is an FDA 510(k)-cleared medical device (K895548) manufactured by Coloplast A/S. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 8, 1990. Regulation: 8.