Liquichek Ethanol/Ammonia Control Level 1 - Indonesia BPOM Medical Device Registration
Liquichek Ethanol/Ammonia Control Level 1 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101222291. 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.
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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
BIORAD LABOARTORIES INC.Country of Origin
United States
Authorized Representative
DIASTIKA BIOTEKINDOAR Address
Rukan Sentra Pemuda Kav.30 - 31 Jalan Pemuda No.61 RT.009 RW.003 Kel. Rawamangun Kec.Pulogadung
Registration Date
Dec 20, 2022
Expiry Date
May 31, 2025
Product Type
Clinical Chemistry Test System
Quality control material (assayed and unassayed) (cair)
Invitro Diagnostics
MGI Universal Sequencing Reaction Kit
WUHAN MGI TECH CO.,LTD
MGI Universal Sequencing Reaction Kit
WUHAN MGI TECH CO.,LTD
MGI DNA Sequencing Library Preparation System
WUHAN MGI TECH CO.,LTD
MGI Genetic Sequencer
WUHAN MGI TECH CO.,LTD
MGI Genetic Sequencer
WUHAN MGI TECH CO.,LTD
MGI Genetic Sequencer
WUHAN MGI TECH CO.,LTD
ORTHO Pooled Screening Cells
ORTHO-CLINICAL DIAGNOSTICS INC.,
ORTHO Vision Analyzer
TECAN SCHWEIZ AG
ORTHO Anti-Human Globulin Anti-lgG (Rabbit) (Green) Ortho BioVue System (IgG Cassette)
ORTHO-CLINICAL DIAGNOSTICS
ORTHO Affirmagen
ORTHO-CLINICAL DIAGNOSTICS INC.,

