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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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BPOM Registered
Risk Class Kelas Resiko : C
ICHROMA™ AFP
Analysis ID: AKL 20306320328

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

BODITECH WITH INC.

Country of Origin

Korea

Authorized Representative

ZOE PELITA NUSANTARA

AR 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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