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BELLAST L24 Cross-Linked Hyaluronic Acid - Indonesia BPOM Medical Device Registration

BELLAST L24 Cross-Linked Hyaluronic Acid is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602913713. The device is manufactured by DONGKOOK PHARMACEUTICALS CO.,LTD from Korea, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. DIAN LANGGENG PRATAMA.

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
BELLAST L24 Cross-Linked Hyaluronic Acid
Analysis ID: AKL 31602913713

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Korea

Authorized Representative

PT. DIAN LANGGENG PRATAMA

AR Address

Jl. Raden Saleh Raya No. 4

Registration Date

Apr 19, 2021

Expiry Date

Feb 18, 2024

Product Type

Prosthetic Surgical Equipment

Dermal filler

Non Electromedic Sterile

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