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SKYLA ™ Hi CRP Reagent Kit - Indonesia BPOM Medical Device Registration

SKYLA ™ Hi CRP Reagent Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305220210. The device is manufactured by SKYLA CORPORATION HSINCHU SCIENCE PARK BRANCH from Taiwan (China), and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. RAFA TOPAZ MAIN.

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BPOM Registered
Risk Class Kelas Resiko : B
SKYLA ™ Hi CRP Reagent Kit
Analysis ID: AKL 20305220210

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Taiwan (China)

Authorized Representative

PT. RAFA TOPAZ MAIN

AR Address

Taman Buaran Indah I Blok U No. 242 Jl. Radin Inten II, Klender, Jakarta Timur

Registration Date

Jun 13, 2022

Expiry Date

Jun 01, 2024

Product Type

Immunological Test System

C-reactive protein immunological test system.

Invitro Diagnostics

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DJ Fang

DJ Fang

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