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NEAUVIA Intense Flux - Indonesia BPOM Medical Device Registration

NEAUVIA Intense Flux is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602420023. The device is manufactured by MATEX LAB SPA from Italy, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. REGENESIS 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 : D
NEAUVIA Intense Flux
Analysis ID: AKL 31602420023

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

MATEX LAB SPA

Country of Origin

Italy

Authorized Representative

PT. REGENESIS INDONESIA

AR Address

Jalan Sultan Iskandar Muda No. 7 A dan B, Kebayoran lama Selatan, Kebayoran Lama, Jakarta Selatan

Registration Date

Apr 24, 2024

Expiry Date

Mar 15, 2028

Product Type

Prosthetic Surgical Equipment

Dermal filler

Non Electromedic Sterile

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