GEOMED Kerrison Forceps - Indonesia BPOM Medical Device Registration

GEOMED Kerrison Forceps is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11103220112. The device is manufactured by GEOMED MEDIZIN-TECHNIK GMBH & CO., KG. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ARTHA MEDIKA SENTOSA.

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