
Latexx Partners Bhd.
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NON-CHLORINATED, POLYMER COATED POWDER-FREE NITRILE PATIENT EXAMINATION GLOVES is an FDA 510(k)-cleared medical device (K011792) manufactured by Latexx Partners Bhd.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 31, 2001. Regulation: 8.

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