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NEAUVIA Organic Stimulate - Indonesia BPOM Medical Device Registration

NEAUVIA Organic Stimulate is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602716793. The device is manufactured by MATEX LAB S.P.A. 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 Organic Stimulate
Analysis ID: AKL 31602716793

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

MATEX LAB S.P.A.

Country of Origin

Italy

Authorized Representative

PT. REGENESIS INDONESIA

AR Address

Jl. Panglima Polim Raya Blok B III/107, Jakarta Selatan

Registration Date

Mar 27, 2020

Expiry Date

Dec 05, 2024

Product Type

Prosthetic Surgical Equipment

Dermal filler

Non Electromedic Sterile

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