Pure Global

NASALIN Baby Daily Nasal Hygiene Microdiffusion - Indonesia BPOM Medical Device Registration

NASALIN Baby Daily Nasal Hygiene Microdiffusion is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20704220014. The device is manufactured by GILBERT LABORATORIES from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BRIDGE TWO.

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 : B
NASALIN Baby Daily Nasal Hygiene Microdiffusion
Analysis ID: AKL 20704220014

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

France

Authorized Representative

PT. BRIDGE TWO

AR Address

Petojo Melintang No. 17 Kel. Petojo Selatan, Kec. Gambir Jakarta Pusat

Registration Date

Apr 01, 2022

Expiry Date

Mar 23, 2026

Product Type

Therapeutic Ear, Nose and Throat Equipment

Nasal irrigation solution

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing