KAZAMA ENT Unit - Indonesia BPOM Medical Device Registration
KAZAMA ENT Unit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10704220024. The device is manufactured by KAZAMAENT CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. DEMKA SAKTI.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
KAZAMAENT CO., LTD.Country of Origin
Korea
Authorized Representative
PT. DEMKA SAKTIAR Address
Jl. Tanah Abang III No. 19 A - B, Jakarta Pusat
Registration Date
Jun 14, 2022
Expiry Date
May 01, 2026
Product Type
Therapeutic Ear, Nose and Throat Equipment
Ear, nose, and throat examination and treatment unit.
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