Pure Global

DEMEDITEC Measles IgM ELISA - Indonesia BPOM Medical Device Registration

DEMEDITEC Measles IgM ELISA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303022556. The device is manufactured by DEMEDITEC DIAGNOSTICS GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FRIMUST ADIJAYA 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
DEMEDITEC Measles IgM ELISA
Analysis ID: AKL 20303022556

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. FRIMUST ADIJAYA UTAMA

AR Address

Jalan Pemuda No. M3, Rt. 002/015, Rawamangun, Pulo Gadung

Registration Date

May 06, 2020

Expiry Date

Apr 09, 2024

Product Type

Serological Reagents

Rubeola (measles) virus serological reagents.

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing