Pure Global

FINECARE™ FIA Meter II Plus SE - Indonesia BPOM Medical Device Registration

FINECARE™ FIA Meter II Plus SE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20304520008. The device is manufactured by GUANGZHOU WONDFO BIOTECH CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. CIPTA VARIA KHARISMA UTAMA.

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
FINECARE™ FIA Meter II Plus SE
Analysis ID: AKL 20304520008

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. CIPTA VARIA KHARISMA UTAMA

AR Address

Jl. Utan Kayu Raya No. 105A Jakarta

Registration Date

Jan 24, 2025

Expiry Date

Sep 04, 2029

Product Type

Immunology Laboratory Equipment and Reagents

Immunofluorometer equipment

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing