Pure Global

ZENIX ZS-Ref Ref Filling Solution - Indonesia BPOM Medical Device Registration

ZENIX ZS-Ref Ref Filling Solution is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101123902. The device is manufactured by GENRUI BIOTECH INC from China, and is classified as Risk Class Kelas Resiko : C. 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 : C
ZENIX ZS-Ref Ref Filling Solution
Analysis ID: AKL 20101123902

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

GENRUI BIOTECH INC

Country of Origin

China

Authorized Representative

PT. SUMIFIN CITRA ABADI

AR Address

Ruko Banjar Wijaya Blok B1 No. 7 Kel. Poris Plawad Indah, Kec. Cipondoh, Tangerang, Banten

Registration Date

Jul 02, 2021

Expiry Date

Apr 15, 2024

Product Type

Clinical Chemistry Test System

Multi parameter clinical chemistry test system

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing