ALIFAX Latex Calibrator - Indonesia BPOM Medical Device Registration
ALIFAX Latex Calibrator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208817341. The device is manufactured by ALIFAX S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MULTISERA INDOSA.
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
ALIFAX S.R.L.Country of Origin
Italy
Authorized Representative
PT. MULTISERA INDOSAAR Address
Jl. Jend. Sudirman No. 689 RT 21 RW 007
Registration Date
Oct 21, 2024
Expiry Date
Dec 31, 2026
Product Type
Hematological Reagents
Hematology quality control mixture.
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