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HONKON High Intensity Focused Ultrasound - Indonesia BPOM Medical Device Registration

HONKON High Intensity Focused Ultrasound is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603122956. The device is manufactured by BEIJING HONKON TECHNOLOGIES CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is INDONESIAN BEAUTY WORLD.

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 : B
HONKON High Intensity Focused Ultrasound
Analysis ID: AKL 21603122956

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

INDONESIAN BEAUTY WORLD

AR Address

Jalan. KH. Samanhudi no 17, Kel. Pasar Baru, Kec. Sawah Besar

Registration Date

May 21, 2021

Expiry Date

Nov 25, 2025

Product Type

Surgical Equipment

Focused ultrasound stimulator system for aesthetic use

Non Radiation Electromedics

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