Pure Global

EVANCARE One Step Rapid Test Dengue IgG/IgM - Indonesia BPOM Medical Device Registration

EVANCARE One Step Rapid Test Dengue IgG/IgM is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303321029. The device is manufactured by SAFECARE BIOTECH (HANGZHOU) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. META MEDICAL TECHNOLOGY.

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
EVANCARE One Step Rapid Test Dengue IgG/IgM
Analysis ID: AKL 20303321029

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. META MEDICAL TECHNOLOGY

AR Address

META TEKNOLOGI MEDIKA

Registration Date

Mar 15, 2023

Expiry Date

Oct 26, 2025

Product Type

Serological Reagents

Dengue virus serological reagents

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing