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AIRBLEND Heated Humidifier System - Indonesia BPOM Medical Device Registration

AIRBLEND Heated Humidifier System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403126703. The device is manufactured by AIRBLEND MEDICAL DEVICE MANUFACTURING INC from Turkey, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FA ANTARES MEDIKA.

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 : B
AIRBLEND Heated Humidifier System
Analysis ID: AKL 20403126703

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Turkey

Authorized Representative

PT. FA ANTARES MEDIKA

AR Address

Ruko Golden Boulevard Blok i No 7 BSD City

Registration Date

Nov 08, 2021

Expiry Date

May 31, 2024

Product Type

Therapeutic Anesthesia Equipment

High flow humidified oxygen delivery device.

Non Radiation Electromedics

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