SEBIA ANTISERA AND FIXATIVE IF - Indonesia BPOM Medical Device Registration

SEBIA ANTISERA AND FIXATIVE IF is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305321033. The device is manufactured by SEBIA from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PROSPEROUS ADVANCED ERA.

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