ULTRA V EZ CANNULA Double COG PDO - Indonesia BPOM Medical Device Registration

ULTRA V EZ CANNULA Double COG PDO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603324978. The device is manufactured by SKIN MEDIENCE CO. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. REGENESIS INDONESIA.

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