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AIRSENSE 10 Autoset for Her - Indonesia BPOM Medical Device Registration

AIRSENSE 10 Autoset for Her is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403913942. 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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BPOM Registered
Risk Class Kelas Resiko : C
AIRSENSE 10 Autoset for Her
Analysis ID: AKL 20403913942

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

Feb 17, 2024

Expiry Date

Aug 22, 2028

Product Type

Therapeutic Anesthesia Equipment

Noncontinuous ventilator (IPPB).

Non Radiation Electromedics

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