TEKNO Reflex Hammer - Indonesia BPOM Medical Device Registration

TEKNO Reflex Hammer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11001126700. The device is manufactured by TEKNO-MEDICAL OPTIC-CHIRURGIE GMBH., GERMANY from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. TRIGELS INDONESIA.

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