TECHLAB C. DIFF QUIK CHEK COMPLETE - Indonesia BPOM Medical Device Registration
TECHLAB C. DIFF QUIK CHEK COMPLETE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303220453. 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 29, 2024
Expiry Date
May 08, 2027
Product Type
Serological Reagents
Clostridium difficile toxin gene amplification assay
Invitro Diagnostics
ALLPLEXโข GI-Parasite Assay
SEEGENE INC.
ALLPLEXโข Respiratory Panel 1A
SEEGENE INC.
ALLPLEXโข GI-Bacteria(II) Assay
SEEGENE INC.
MGI Nucleic Acid Extraction Kit
WUHAN MGI TECH CO.,LTD
Allplexโข GI-Virus Assay
SEEGENE INC.
AllplexTM GI-Bacteria (I) Assay
SEEGENE INC.
ALLPLEXโข Meningitis-B Assay
SEEGENE INC.
ALLPLEXโข Meningitis-V1 Assay
SEEGENE INC.
ALLPLEXโข Meningitis-V2 Assay
SEEGENE INC.
AllplexTM Respiratory Panel 3
SEEGENE INC.

