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PLURYAL Densify - Indonesia BPOM Medical Device Registration

PLURYAL Densify is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602320142. The device is manufactured by MD SKIN SOLUTIONS from Luxembourg, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. ETERNAL VAST OCEAN.

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
PLURYAL Densify
Analysis ID: AKL 31602320142

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

MD SKIN SOLUTIONS

Country of Origin

Luxembourg

Authorized Representative

PT. ETERNAL VAST OCEAN

AR Address

Jl. Tanah Abang IV No. 34B, RT 004 / RW 03, Gambir, Jakarta Pusat

Registration Date

Feb 07, 2023

Expiry Date

Dec 31, 2024

Product Type

Prosthetic Surgical Equipment

Dermal filler

Non Electromedic Sterile

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