MEPILEX Border Post-Op - Indonesia BPOM Medical Device Registration

MEPILEX Border Post-Op is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603422341. The device is manufactured by MöLNLYCKE HEALTH CARE AB from Sweden, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDI KHARISMA INTERNATIONAL.

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