Pure Global

NEWPONG SONOQUEEN Focused Ultrasound Stimulator - Indonesia BPOM Medical Device Registration

NEWPONG SONOQUEEN Focused Ultrasound Stimulator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603912374. The device is manufactured by NEWPONG CO.,LTD from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDIVA.

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
NEWPONG SONOQUEEN Focused Ultrasound Stimulator
Analysis ID: AKL 21603912374

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

NEWPONG CO.,LTD

Country of Origin

Korea

Authorized Representative

PT. MEDIVA

AR Address

K-LINK TOWER, LEVEL 11, SUITE G. JL. Jend. Gatot Subroto Kav. 59A

Registration Date

Dec 12, 2021

Expiry Date

Oct 15, 2024

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