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AMALIAN III Expert Volume - Indonesia BPOM Medical Device Registration

AMALIAN III Expert Volume is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602320198. The device is manufactured by S&V TECHNOLOGIES GMBH from Germany, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. OBSERVING THE MEDICAL FAMILY.

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 : D
AMALIAN III Expert Volume
Analysis ID: AKL 31602320198

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Germany

Authorized Representative

PT. OBSERVING THE MEDICAL FAMILY

AR Address

PERMATA SENAYAN RUKAN E/01 Jl. Tentara Pelajar

Registration Date

May 26, 2023

Expiry Date

Oct 29, 2025

Product Type

Prosthetic Surgical Equipment

Dermal filler

Non Electromedic Sterile

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