ULTRAFLEX™ Intra-Aortic Balloon Catheters - Indonesia BPOM Medical Device Registration

ULTRAFLEX™ Intra-Aortic Balloon Catheters is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503818464. The device is manufactured by ARROW INTERNATIONAL, LLC. from United States, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MULTIDAYA MEDIKA.

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