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ASTRAL 150 - Indonesia BPOM Medical Device Registration

ASTRAL 150 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403916552. The device is manufactured by RESMED PTY., LTD. from Australia, 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
ASTRAL 150
Analysis ID: AKL 20403916552

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

RESMED PTY., LTD.

Country of Origin

Australia

Authorized Representative

PT. QUALTEK CONSULTANT JAKARTA

AR Address

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

Registration Date

Dec 28, 2023

Expiry Date

Aug 22, 2028

Product Type

Therapeutic Anesthesia Equipment

Continuous ventilator.

Non Radiation Electromedics

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