Pure Global

INTERSURGICAL nFlow™ Infant Nasal CPAP - Indonesia BPOM Medical Device Registration

INTERSURGICAL nFlow™ Infant Nasal CPAP is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403023128. The device is manufactured by INTERSURGICAL LIMITED. from United Kingdom, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MADESA SEJAHTERA UTAMA.

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 : A
INTERSURGICAL nFlow™ Infant Nasal CPAP
Analysis ID: AKL 10403023128

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

United Kingdom

Authorized Representative

PT. MADESA SEJAHTERA UTAMA

AR Address

JL. GUNUNG SAHARI RAYA 51- A NO.14

Registration Date

Jul 24, 2021

Expiry Date

Mar 10, 2024

Product Type

Therapeutic Anesthesia Equipment

Breathing tube support.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing