Coloplast Corp.
SpeediCath Flex Coude
SKU K161672UPC GBM
In Stock
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IIFDA 510(k) Cleared (K161672)
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Free shipping on orders over $99 · 30-day returns
Coloplast Corp.
Free shipping on orders over $99 · 30-day returns
SpeediCath Flex Coude is an FDA 510(k)-cleared medical device (K161672) manufactured by Coloplast Corp.. 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 September 28, 2016. Regulation: 8.
