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Profacial - Indonesia BPOM Medical Device Registration

Profacial is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603422104. The device is manufactured by SEOULINE MEDICARE CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. EULOGY ASIA 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
Profacial
Analysis ID: AKL 21603422104

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Korea

Authorized Representative

PT. EULOGY ASIA INDONESIA

AR Address

Jl. Cideng Barat No. 64 #02-02, RT 014, RW 002, Kec. Gambir, Kel. Cideng

Registration Date

Sep 10, 2024

Expiry Date

Jul 01, 2029

Product Type

Surgical Equipment

Focused ultrasound stimulator system for aesthetic use

Non Radiation Electromedics

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