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PLURYAL® Booster - Indonesia BPOM Medical Device Registration

PLURYAL® Booster is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602914380. The device is manufactured by CROMA GMBH from Austria, 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® Booster
Analysis ID: AKL 31602914380

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

CROMA GMBH

Country of Origin

Austria

Authorized Representative

PT. ETERNAL VAST OCEAN

AR Address

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

Registration Date

Nov 11, 2021

Expiry Date

Sep 24, 2025

Product Type

Prosthetic Surgical Equipment

Dermal filler

Non Electromedic Sterile

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