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GENRUI ALP Reagent Kit (IFCC Kinetic Method) - Indonesia BPOM Medical Device Registration

GENRUI ALP Reagent Kit (IFCC Kinetic Method) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101220771. The device is manufactured by GENRUI BIOTECH INC. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MEGA PRATAMA MEDICALINDO.

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.

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BPOM Registered
Risk Class Kelas Resiko : B
GENRUI ALP Reagent Kit (IFCC Kinetic Method)
Analysis ID: AKL 20101220771

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

MEGA PRATAMA MEDICALINDO

AR Address

Jl. Pluit Raya 133 Blok A.3

Registration Date

Jun 10, 2022

Expiry Date

Jul 27, 2026

Product Type

Clinical Chemistry Test System

Alkaline phosphatase or isoenzymes test system (kit & cair)

Invitro Diagnostics

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