SERENITY Emergency Treatment Unit - Indonesia BPOM Medical Device Registration

SERENITY Emergency Treatment Unit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603113388. The device is manufactured by DOCTORS FRIEND MEDICAL INSTRUMENT CO. LTD. from Taiwan (China), and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SERENITY INDONESIA.

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