AFIAS Total IgE - Indonesia BPOM Medical Device Registration
AFIAS Total IgE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305420528. 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
Oct 28, 2024
Expiry Date
Feb 05, 2029
Product Type
Immunological Test System
Immunoglobulins A, G, M, D, and E immunological test system.
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