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Dermashine Pro - Indonesia BPOM Medical Device Registration

Dermashine Pro is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903028254. The device is manufactured by PANACE CO.,LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SMELL 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 : B
Dermashine Pro
Analysis ID: AKL 20903028254

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

PANACE CO.,LTD.

Country of Origin

Korea

Authorized Representative

SMELL MEDICAL INDONESIA

AR Address

Gd. Graha Mampang lt. 2. Jl. Mampang Prapatan Raya no. 100 Duren Tiga Pancoran

Registration Date

Dec 29, 2020

Expiry Date

Oct 23, 2025

Product Type

General Hospital Equipment and Other Individuals

Syringe needle introducer.

Non Radiation Electromedics

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