PROLINE - b CK-MB FS - Indonesia BPOM Medical Device Registration

PROLINE - b CK-MB FS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101713439. The device is manufactured by DIASYS DIAGNOSTIC SYSTEMS, GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PRODIA DIAGNOSTIC LINE.

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