AFIAS PRL - Indonesia BPOM Medical Device Registration
AFIAS PRL is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101128947. The device is manufactured by BODITECH WITH INC. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TRIPATRIA MAINSTAY MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BODITECH WITH INC.Country of Origin
Korea
Authorized Representative
PT. TRIPATRIA MAINSTAY MEDIKAAR Address
Jl Musi No. 37 Jakarta 10150
Registration Date
Dec 31, 2021
Expiry Date
Apr 01, 2024
Product Type
Clinical Chemistry Test System
Prolactin (lactogen) test system (card)
Invitro Diagnostics
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