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LAFULLEN - Indonesia BPOM Medical Device Registration

LAFULLEN is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602320187. The device is manufactured by SAMYANG HOLDINGS CORPORATION from Korea, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. HAJU MEDICAL 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
LAFULLEN
Analysis ID: AKL 31602320187

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Korea

Authorized Representative

PT. HAJU MEDICAL INDONESIA

AR Address

Gedung Tifa Arum Realty Lt.8, Suite 801 Jl. Kuningan Barat 1 No. 26, Kelurahan Kuningan Barat, Kecamatan Mampang Prapatan. Jakarta Selatan, DKI Jakarta

Registration Date

Dec 06, 2023

Expiry Date

Nov 25, 2027

Product Type

Prosthetic Surgical Equipment

Dermal filler

Non Electromedic Sterile

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