CITEST - Multi-Drug 3 Drugs Rapid Test Cassette (Urine) (MOP300/AMP1000/THC50) - Indonesia BPOM Medical Device Registration
CITEST - Multi-Drug 3 Drugs Rapid Test Cassette (Urine) (MOP300/AMP1000/THC50) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20103420208. The device is manufactured by CITEST DIAGNOSTICS INC from Canada, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is CAKRA MEDIKA UTAMA.
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
CITEST DIAGNOSTICS INCCountry of Origin
Canada
Authorized Representative
CAKRA MEDIKA UTAMAAR Address
FORESTA BUSINESS LOFT 6 No. 10, Jl. Raya Boulevard Utara BSD City, Desa/Kelurahan Lengkong Kulon
Registration Date
Jul 31, 2024
Expiry Date
Mar 25, 2027
Product Type
Clinical Toxicology Test System
Multi parameter clinical toxicology test system
Invitro Diagnostics
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