AFIAS Tn-I Plus - Indonesia BPOM Medical Device Registration
AFIAS Tn-I Plus is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101120402. 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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Risk Classification
Product Class
Kelas : 2
Manufacturer
BODITECH WITH INC.Country of Origin
Korea
Authorized Representative
TRIPATRIA MAINSTAY MEDIKAAR Address
Jl Musi No. 37 Jakarta 10150
Registration Date
Nov 28, 2021
Expiry Date
Apr 01, 2024
Product Type
Clinical Chemistry Test System
Creatine phosphokinase/creatine kinase or isoenzymes test system(kit & cair)
Invitro Diagnostics
AFIAS Ferritin
AFIAS Tn-I Plus
BODITECH Free T4 Control
AFIAS AMH
ICHROMA™ M3
AFIAS 6 reader and Accessories
AFIAS Microalbumin
AFIAS Free T4
BODITECH Troponin T Control
ICHROMA™ CK-MB
COMPEX WIRELESS MUSCLE STIMULATOR
DOMEX TECHNOLOGY CORPORATION
COSMED Q-NRG+
COSMED S.R.L
COSMED Quark RMR
COSMED S.R.L.
COSMED Q-BOX Body Plethysmography
COSMED S.R.L.
COSMED Quark PFT
COSMED S.R.L.
COSMED Quark CPET
COSMED S.R.L.
LODE Angio Imaging - with Stress Support Radiology
LODE B.V.
LODE Cardiac Rehab Manager (LCRM)
LODE B.V.
AFIAS IL-6
BODITECH WITH INC.
AFIAS EAA
BODITECH WITH INC