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Hyaldew Fine - Indonesia BPOM Medical Device Registration

Hyaldew Fine is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602811635. The device is manufactured by BIOPLUS CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. HERCA CIPTA DERMAL PERDANA.

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
Hyaldew Fine
Analysis ID: AKL 31602811635

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

BIOPLUS CO., LTD.

Country of Origin

Korea

Authorized Representative

PT. HERCA CIPTA DERMAL PERDANA

AR Address

Taman Harapan Indah Blok FF 1 B No. 10 Kel. Jelambar Baru, Kec. Grogol Petamburan Jakarta Barat 11460

Registration Date

Sep 08, 2022

Expiry Date

Jul 12, 2025

Product Type

Prosthetic Surgical Equipment

Dermal filler

Non Electromedic Sterile

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