Pure Global

NEURAMIS® Deep - Indonesia BPOM Medical Device Registration

NEURAMIS® Deep is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602125581. The device is manufactured by MEDYTOX INC. 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : D
NEURAMIS® Deep
Analysis ID: AKL 31602125581

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

MEDYTOX INC.

Country of Origin

Korea

Authorized Representative

PT. HAJU MEDICAL INDONESIA

AR Address

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

Registration Date

Sep 16, 2021

Expiry Date

Apr 01, 2026

Product Type

Prosthetic Surgical Equipment

Dermal filler

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing