Pure Global

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
LIQUIZONE Alkaline Phosphatase
Analysis ID: AKL 20101814778

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

PT. SUMIFIN CITRA ABADI

AR 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)

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing