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AFIAS Microalbumin - Indonesia BPOM Medical Device Registration

AFIAS Microalbumin is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101812469. 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 TRIPATRIA MAINSTAY MEDIKA.

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BPOM Registered
Risk Class Kelas Resiko : B
AFIAS Microalbumin
Analysis ID: AKL 20101812469

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

BODITECH WITH INC.

Country of Origin

Korea

Authorized Representative

TRIPATRIA MAINSTAY MEDIKA

AR Address

Jl Musi No. 37 Jakarta 10150

Registration Date

Dec 25, 2021

Expiry Date

Apr 01, 2024

Product Type

Clinical Chemistry Test System

Albumin test system (card)

Invitro Diagnostics

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