AFIAS AMH - Indonesia BPOM Medical Device Registration
AFIAS AMH is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101420587. 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 PT. BODITECH MED INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BODITECH WITH 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 31, 2024
Expiry Date
Nov 06, 2028
Product Type
Clinical Chemistry Test System
Human growth hormone test system (kit & cair)
Invitro Diagnostics
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