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AirFit N20 Nasal Mask System - Indonesia BPOM Medical Device Registration

AirFit N20 Nasal Mask System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403420126. The device is manufactured by RESMED ASIA PTE., LTD. from Singapore, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. QUALTEK CONSULTANT JAKARTA.

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 : C
AirFit N20 Nasal Mask System
Analysis ID: AKL 20403420126

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Singapore

Authorized Representative

PT. QUALTEK CONSULTANT JAKARTA

AR Address

Icon Business Park Blok K No 6, BSD City, Kab Tangerang, Banten

Registration Date

Feb 21, 2024

Expiry Date

Aug 22, 2028

Product Type

Therapeutic Anesthesia Equipment

Positive airway pressure delivery system

Non Electromedic Non Sterile

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