Pure Global

NAISSA T4 - Indonesia BPOM Medical Device Registration

NAISSA T4 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101222279. The device is manufactured by NEOMEDICA DOO from Serbia, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FLEXYLABS INSTRUMENT INDONESIA.

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
NAISSA T4
Analysis ID: AKL 20101222279

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

NEOMEDICA DOO

Country of Origin

Serbia

Authorized Representative

PT. FLEXYLABS INSTRUMENT INDONESIA

AR Address

Ruko Poris Garden Blok A9A No.1A

Registration Date

Dec 19, 2022

Expiry Date

Oct 27, 2026

Product Type

Clinical Chemistry Test System

Free thyroxine test system (kit & cair)

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing