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AIRSENSE 10 Autoset FH APAC TRI C - Indonesia BPOM Medical Device Registration

AIRSENSE 10 Autoset FH APAC TRI C is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403220548. 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.

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Risk Class Kelas Resiko : C
AIRSENSE 10 Autoset FH APAC TRI C
Analysis ID: AKL 20403220548

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

Aug 19, 2022

Expiry Date

Oct 14, 2026

Product Type

Therapeutic Anesthesia Equipment

Positive airway pressure delivery system

Non Radiation Electromedics

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