LDM Triple - Indonesia BPOM Medical Device Registration

LDM Triple is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603420835. The device is manufactured by WELLCOMET GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. HAJU MEDICAL INDONESIA.

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