AESCULAP FI Camera Control Unit - Indonesia BPOM Medical Device Registration

AESCULAP FI Camera Control Unit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801320564. The device is manufactured by AESCULAP AG. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. B. BRAUN MEDICAL INDONESIA.

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