PERMEADERM Biosynthetic Wound Matrix - Indonesia BPOM Medical Device Registration

PERMEADERM Biosynthetic Wound Matrix is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31603520153. The device is manufactured by TRELLEBORG SEALING SOLUTIONS US, INC. from United States, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. ANDAMAN MEDICAL INDONESIA.

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