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N.S. Uni-Gloves Sdn. Bhd.
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UNIGLOVE NITRILE POWDERED EXAMINATION GLOVES is an FDA 510(k)-cleared medical device (K000688) manufactured by N.S. Uni-Gloves Sdn. Bhd.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 11, 2000. Regulation: 8.

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