LIQUIZONE Alkaline Phosphatase - Indonesia BPOM Medical Device Registration
LIQUIZONE Alkaline Phosphatase is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101814778. The device is manufactured by MEDSOURCE OZONE BIOMEDICALS PVT., LTD. from India, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SUMIFIN CITRA ABADI.
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
MEDSOURCE OZONE BIOMEDICALS PVT., LTD.Country of Origin
India
Authorized Representative
PT. SUMIFIN CITRA ABADIAR Address
Jl. Alam Sutera Boulevard Alam Sutera Town Center (ASTC) Blok 10D No.19, Kel. Pakulonan, Kec. Serpong Utara - Tangerang Selatan 15325
Registration Date
Oct 14, 2024
Expiry Date
May 22, 2029
Product Type
Clinical Chemistry Test System
Alkaline phosphatase or isoenzymes test system (kit & cair)
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