Pure Global

NOVALISA Entamoeba Histolytica IgG - Indonesia BPOM Medical Device Registration

NOVALISA Entamoeba Histolytica IgG is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303612862. The device is manufactured by NOVATEC IMMUDIAGNOSTICA GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BESTARI SUKSES MAKMUR.

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
NOVALISA Entamoeba Histolytica IgG
Analysis ID: AKL 20303612862

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. BESTARI SUKSES MAKMUR

AR Address

Kokan Permata Kelapa Gading Blok E No. 5 Jl. Boulevard Bukit Gading Raya, Kel. Gading Barat, Kec. Kelapa Gading, Jakarta Utara

Registration Date

May 25, 2022

Expiry Date

Aug 31, 2024

Product Type

Serological Reagents

Entamoeba histolytica serological reagents.

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from NOVATEC IMMUDIAGNOSTICA GMBH.
Products from the same manufacturer (2 products)