ICHROMA™ AFP - Indonesia BPOM Medical Device Registration
ICHROMA™ AFP is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20306320328. The device is manufactured by BODITECH WITH INC. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is ZOE PELITA NUSANTARA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BODITECH WITH INC.Country of Origin
Korea
Authorized Representative
ZOE PELITA NUSANTARAAR Address
JALAN CIKINI II NO 8 B
Registration Date
Nov 08, 2023
Expiry Date
Oct 01, 2027
Product Type
Tumor Antigen Immunologic Test System
AFP-L3% immunological test system.
Invitro Diagnostics
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