DEFIGARD 5000 - Indonesia BPOM Medical Device Registration

DEFIGARD 5000 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505712268. The device is manufactured by SCHILLER MEDICAL SAS. from France, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MULYA HUSADA JAYA.

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