KOWA Non-Mydriatic Retinal Camera - Indonesia BPOM Medical Device Registration
KOWA Non-Mydriatic Retinal Camera is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21201614046. The device is manufactured by KOWA COMPANY, LTD. CHOFU FACTORY. from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TRIASTRI MEDITAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
KOWA COMPANY, LTD. CHOFU FACTORY.Country of Origin
Japan
Authorized Representative
PT. TRIASTRI MEDITAMAAR Address
GRIYA KEMAYORAN BLOK R-41 JL. INDUSTRI RAYA NO. 9-11
Registration Date
Jan 25, 2022
Expiry Date
Dec 31, 2026
Product Type
Diagnostic Eye Equipment
Opthalmic camera.
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