STRYKER CrossFlow® Integrated Arthroscopy Pump - Indonesia BPOM Medical Device Registration

STRYKER CrossFlow® Integrated Arthroscopy Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21301910151. The device is manufactured by STRYKER ENDOSCOPY. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TRANSMEDIC INDONESIA.

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