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Sygmalift - Indonesia BPOM Medical Device Registration

Sygmalift is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603323194. The device is manufactured by MEDIXSYSTEME AG from Liechtenstein, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. AESENDIA INFINI 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
Sygmalift
Analysis ID: AKL 21603323194

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

MEDIXSYSTEME AG

Country of Origin

Liechtenstein

Authorized Representative

PT. AESENDIA INFINI INDONESIA

AR Address

AESENDIA INFINI INDONESIA

Registration Date

Feb 07, 2023

Expiry Date

Sep 30, 2024

Product Type

Surgical Equipment

Focused ultrasound stimulator system for aesthetic use

Non Radiation Electromedics

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