CONDALAB Columbia Agar Base EP/USP/ISO - Indonesia BPOM Medical Device Registration
CONDALAB Columbia Agar Base EP/USP/ISO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10302220139. The device is manufactured by LABORATORIOS CONDA S.A. from Spain, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. GANDASARI EKASATYA.
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 : 1
Manufacturer
LABORATORIOS CONDA S.A.Country of Origin
Spain
Authorized Representative
PT. GANDASARI EKASATYAAR Address
Jl. Raya HANKAM No.9A RT.007/002 Kel. Bambu Apus, Kec. Cipayung 13890
Registration Date
Oct 12, 2022
Expiry Date
Jun 17, 2027
Product Type
Microbiology Equipment
Microbiological assay culture medium.
Invitro Diagnostics
CONDALAB Nutrient Agar ISO
Condalab King B Medium (Pseudomonas F agar) ISO
CONDALAB Cetrimide Agar Base EP/USP/ISO
CONDALAB R2A Agar EP/USP
CONDALAB MacConkey Broth EP/USP
CONDALAB Sabouraud Dextrose Agar EP/USP/ISO
Condalab Trypticasein Soy Agar (TSA) EP/USP/ISO
CONDALAB Bismuth Sulfite Agar (Wilson Blair) USP
CONDALAB MacConkey Agar EP / USP / ISO
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