PENTAX MEDICAL Fiberoptic Naso-Pharyngo-Laryngoscope - Indonesia BPOM Medical Device Registration

PENTAX MEDICAL Fiberoptic Naso-Pharyngo-Laryngoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20703912141. The device is manufactured by HOYA CORPORATION PENTAX Miyagi from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PRO-HEALTH INTERNATIONAL.

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