CITEST FT3 Test Cassette (Serum/Plasma) - Indonesia BPOM Medical Device Registration
CITEST FT3 Test Cassette (Serum/Plasma) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101323716. The device is manufactured by CITEST DIAGNOSTICS INC from Canada, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. NELTA MULTI GRACIA.
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
PT. NELTA MULTI GRACIAAR Address
Metland Menteng. Jl. Menteng Niaga Blok J7 No.1 Ujung Menteng, Cakung, Jakarta Timur 13960
Registration Date
Aug 23, 2023
Expiry Date
Feb 20, 2026
Product Type
Clinical Chemistry Test System
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