
Bio D Corp.
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FLUFF UNDERPAD TYPE UP1002 is an FDA 510(k)-cleared medical device (K802730) manufactured by Bio D Corp.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 9, 1980. Regulation: 8.

Ansell
SKU MSC846624

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McKesson
SKU VM-1270030

Hollister
SKU VM-1270031