
Biopro (M) Sdn Bhd
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NITRILON CORRECT-TOUCH is an FDA 510(k)-cleared medical device (K981333) manufactured by Biopro (M) Sdn Bhd. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 21, 1998. Regulation: 8.

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