PULSAR Expandable Cage System Instrument - Indonesia BPOM Medical Device Registration

PULSAR Expandable Cage System Instrument is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303420281. The device is manufactured by GS MEDICAL CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is FAJAR SELARAS PARTNERS.

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