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P.T. Anlis Abadi Internasional
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POWDERED LATEX PATIENT EXAMINATION GLOVES is an FDA 510(k)-cleared medical device (K051465) manufactured by P.T. Anlis Abadi Internasional. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 11, 2005. Regulation: 8.

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