AFIAS PCT Plus G - Indonesia BPOM Medical Device Registration
AFIAS PCT Plus G is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303420107. The device is manufactured by BODITECH MED INC., from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BODITECH MED INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BODITECH MED INC.,Country of Origin
Korea
Authorized Representative
PT. BODITECH MED INDONESIAAR Address
Ruko Alam Sutera, Jalur Sutera Kavling 25 B-C No.1
Registration Date
Mar 22, 2024
Expiry Date
Oct 25, 2028
Product Type
Serological Reagents
Procalcitonin test system
Invitro Diagnostics
AFIAS PSA
AFIAS D-Dimer Neo
AFIAS Cyfra 21-1
AFIAS CRP
AFIAS NT-proBNP
AFIAS TSH
AFIAS PCT X
BODITECH RF IgM Control
BODITECH TSH Plus Control
AFIAS Vitamin D Neo
AFIAS PSA
BODITECH MED INC.,
AFIAS NT-proBNP
BODITECH MED INC.,
AFIAS Cyfra 21-1
BODITECH MED INC.,
AFIAS Ferritin
BODITECH WITH INC.
AFIAS Tn-I Plus
BODITECH WITH INC.
AFIAS D-Dimer Neo
BODITECH MED INC.,
AFIAS CRP
BODITECH MED INC.,
AFIAS TSH
BODITECH MED INC.,
AFIAS PCT X
BODITECH MED INC.,
BODITECH RF IgM Control
BODITECH MED INC.,