GENESIS Rapid Seal II Tube Sealer - Indonesia BPOM Medical Device Registration

GENESIS Rapid Seal II Tube Sealer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10209420244. The device is manufactured by CENTRON TECHNOLOGIES CORP. from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. PRIMA ALKESINDO NUSANTARA.

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