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LIFOTRONIC HIFU (High-Intensity Focused Ultrasound) Device - Indonesia BPOM Medical Device Registration

LIFOTRONIC HIFU (High-Intensity Focused Ultrasound) Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603421354. The device is manufactured by HUNAN LIFOTRONIC MEDICAL TECHNOLOGY CO.,LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is LIFOTRONIC TECHNOLOGY 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 : B
LIFOTRONIC HIFU (High-Intensity Focused Ultrasound) Device
Analysis ID: AKL 21603421354

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

LIFOTRONIC TECHNOLOGY INDONESIA

AR Address

Ruko South Goldfinch Blok SGA No. 17, Jl. Spring Boulevard, Kode Pos 15322, Kel. Cihuni, Kec. Pagedangan, Kab. Tangerang, Provinsi Banten

Registration Date

Jun 24, 2024

Expiry Date

Apr 01, 2029

Product Type

Surgical Equipment

Focused ultrasound stimulator system for aesthetic use

Non Radiation Electromedics

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