AGAPPE LDH-P - Indonesia BPOM Medical Device Registration

AGAPPE LDH-P is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101612860. The device is manufactured by AGAPPE DIAGNOSTIC SWITZERLAND GMBH. from Switzerland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MULTIMEDILAB KARYAMANDIRI.

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