ACER MEDICAL VeriSee DR - Indonesia BPOM Medical Device Registration
ACER MEDICAL VeriSee DR is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21201320247. The device is manufactured by ACER MEDICAL INC. from Taiwan (China), and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. QUALTEK CONSULTANT JAKARTA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ACER MEDICAL INC.Country of Origin
Taiwan (China)
Authorized Representative
PT. QUALTEK CONSULTANT JAKARTAAR Address
Icon Business Park Blok K No 6, BSD City, Kab Tangerang, Banten
Registration Date
Jan 25, 2023
Expiry Date
Oct 19, 2027
Product Type
Diagnostic Eye Equipment
Retinal Diagnostic Software Device
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