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Liquichek Ethanol/Ammonia Control Level 2 - Indonesia BPOM Medical Device Registration

Liquichek Ethanol/Ammonia Control Level 2 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101222268. The device is manufactured by BIORAD LABOARTORIES INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is DIASTIKA BIOTEKINDO.

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BPOM Registered
Risk Class Kelas Resiko : B
Liquichek Ethanol/Ammonia Control Level 2
Analysis ID: AKL 20101222268

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

DIASTIKA BIOTEKINDO

AR Address

Rukan Sentra Pemuda Kav.30 - 31 Jalan Pemuda No.61 RT.009 RW.003 Kel. Rawamangun Kec.Pulogadung

Registration Date

Dec 19, 2022

Expiry Date

May 31, 2025

Product Type

Clinical Chemistry Test System

Quality control material (assayed and unassayed) (cair)

Invitro Diagnostics

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