Pure Global

NEOPAP Neonatal CPAP System - Indonesia BPOM Medical Device Registration

NEOPAP Neonatal CPAP System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403812869. The device is manufactured by CIRCADIANCE, LLC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MAIN COMMERCIAL HOSPI.

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 : C
NEOPAP Neonatal CPAP System
Analysis ID: AKL 20403812869

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

CIRCADIANCE, LLC.

Country of Origin

United States

Authorized Representative

PT. MAIN COMMERCIAL HOSPI

AR Address

JL. TAMAN MEKAR AGUNG NO. 32-33 RT.003-RW.006 KEL. MEKARWANGI, KEC. BOJONGLOA KIDUL - KOTA BANDUNG

Registration Date

Jun 30, 2021

Expiry Date

Feb 18, 2024

Product Type

Therapeutic Anesthesia Equipment

Positive airway pressure delivery system

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing