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DNA Filler Mid - Indonesia BPOM Medical Device Registration

DNA Filler Mid is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602220129. The device is manufactured by SCL CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. ANDALAS AESTHETIC MED.

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
DNA Filler Mid
Analysis ID: AKL 31602220129

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

SCL CO., LTD

Country of Origin

Korea

Authorized Representative

PT. ANDALAS AESTHETIC MED

AR Address

ANDALAS AESTHETIC MED

Registration Date

Dec 21, 2022

Expiry Date

Aug 16, 2025

Product Type

Prosthetic Surgical Equipment

Dermal filler

Non Electromedic Sterile

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