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Liquichek Blood Gas Plus E Control Level 3 - Indonesia BPOM Medical Device Registration

Liquichek Blood Gas Plus E Control Level 3 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101221659. The device is manufactured by BIORAD LABORATORIES, INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DIASTIKA BIOTEKINDO.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : B
Liquichek Blood Gas Plus E Control Level 3
Analysis ID: AKL 20101221659

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. DIASTIKA BIOTEKINDO

AR Address

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

Registration Date

Oct 06, 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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