AFIAS MxA/CRP - Indonesia BPOM Medical Device Registration
AFIAS MxA/CRP is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305420315. 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 BODITECH MED INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BODITECH WITH INCCountry of Origin
Korea
Authorized Representative
BODITECH MED INDONESIAAR Address
Ruko Alam Sutera, Jalur Sutera Kavling 25 B-C No.1
Registration Date
Jul 08, 2024
Expiry Date
Feb 05, 2029
Product Type
Immunological Test System
C-reactive protein immunological test system.
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