TOX A/B QUIK CHEK - Indonesia BPOM Medical Device Registration
TOX A/B QUIK CHEK is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208220167. The device is manufactured by TECHLAB INC from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SCIENCEWERKE.
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
TECHLAB INCCountry of Origin
United States
Authorized Representative
PT. SCIENCEWERKEAR Address
Jl.Palmerah Barat No.25
Registration Date
Jul 05, 2024
Expiry Date
May 08, 2027
Product Type
Hematological Reagents
Hematology quality control mixture.
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