
Dornier Medtech America, Inc.
Free shipping on orders over $99 · 30-day returns
UROTRACT I is an FDA 510(k)-cleared medical device (K955019) manufactured by Dornier Medtech America, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 5, 1995. Regulation: 8.