BE Thrombomate XRA - Indonesia BPOM Medical Device Registration

BE Thrombomate XRA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20205420122. The device is manufactured by KOMMANDITGESELLSCHAFT BEHNK ELEKTRONIK GMBH & CO from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MULTI SARANA MEDIKA.

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