ASCENDA Intratechal Catheter 73 cm Pump Segment Revision Kit - Indonesia BPOM Medical Device Registration

ASCENDA Intratechal Catheter 73 cm Pump Segment Revision Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31002817428. The device is manufactured by MEDTRONIC PUERTO RICO OPERATIONS CO. JUNCOS from United States, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MEDTRONIC INDONESIA.

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