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FREND™ SYSTEM - Indonesia BPOM Medical Device Registration

FREND™ SYSTEM is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10102320460. The device is manufactured by NANOENTEK INC from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is SEGMED DISTRIBUTION 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.

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BPOM Registered
Risk Class Kelas Resiko : A
FREND™ SYSTEM
Analysis ID: AKL 10102320460

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

NANOENTEK INC

Country of Origin

Korea

Authorized Representative

SEGMED DISTRIBUTION INDONESIA

AR Address

SEGMED DISTRIBUSI INDONESIA

Registration Date

Mar 22, 2023

Expiry Date

Oct 27, 2025

Product Type

Clinical Laboratory Equipment

Fluorometer for clinical use.

Invitro Diagnostics

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