AFIAS T3 - Indonesia BPOM Medical Device Registration
AFIAS T3 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101324672. 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 BODITECH MED INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BODITECH MED INC.,Country of Origin
Korea
Authorized Representative
BODITECH MED INDONESIAAR Address
Ruko Alam Sutera, Jalur Sutera Kavling 25 B-C No.1
Registration Date
Dec 29, 2023
Expiry Date
Oct 25, 2028
Product Type
Clinical Chemistry Test System
Total triiodothyronine test system (strip & midstream)
Invitro Diagnostics
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AFIAS CRP
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AFIAS Vitamin D Neo
BODITECH D-Dimer Control
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BODITECH Vitamin D Control
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