Coloplast Corp.
MODIFICATION TO WOUN'DRES
SKU K991202UPC MGQ
In Stock
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FDA 510(k) Cleared (K991202)
1
Free shipping on orders over $99 · 30-day returns
Coloplast Corp.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO WOUN'DRES is an FDA 510(k)-cleared medical device (K991202) manufactured by Coloplast Corp.. This device is classified under the Unknown specialty. FDA Device Class U. FDA clearance granted on June 3, 1999.
Ansell
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