ANYPLUS PLIF PEEK Cage - Indonesia BPOM Medical Device Registration

ANYPLUS PLIF PEEK Cage is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302510183. The device is manufactured by GS MEDICAL CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FAJAR SELARAS PARTNERS.

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