Pure Global

HYZER ME - Indonesia BPOM Medical Device Registration

HYZER ME is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603023951. The device is manufactured by ILOODA CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ZHENGAN 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
HYZER ME
Analysis ID: AKL 21603023951

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

ILOODA CO., LTD.

Country of Origin

Korea

Authorized Representative

ZHENGAN INDONESIA

AR Address

Ruko Duren Sawit Center No. 8E, Jl. Raya Duren Sawit

Registration Date

Jul 16, 2020

Expiry Date

May 13, 2025

Product Type

Surgical Equipment

Focused ultrasound stimulator system for aesthetic use

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from ZHENGAN INDONESIA
Products with the same authorized representative (1 products)