PUROFLEX Ureteral Stent Set - Indonesia BPOM Medical Device Registration

PUROFLEX Ureteral Stent Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805806874. The device is manufactured by BARD ANGIOMED GMBH & CO., MEDIZINRECHNIK KG. from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SCINTILLATING ASIAN CENTER.

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