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AIRFIT N30 - Indonesia BPOM Medical Device Registration

AIRFIT N30 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403126550. 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 N30
Analysis ID: AKL 20403126550

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

Nov 23, 2021

Expiry Date

Mar 31, 2025

Product Type

Therapeutic Anesthesia Equipment

Positive airway pressure delivery system

Non Electromedic Non Sterile

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