AIRFIT N30i Quiet - Indonesia BPOM Medical Device Registration
AIRFIT N30i Quiet is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403122788. 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 Classification
Product Class
Kelas : 2
Manufacturer
RESMED PTY LTDCountry of Origin
Australia
Authorized Representative
PT. QUALTEK CONSULTANT JAKARTAAR Address
Icon Business Park Blok K No 6, BSD City, Kab Tangerang, Banten
Registration Date
May 18, 2021
Expiry Date
Mar 30, 2026
Product Type
Therapeutic Anesthesia Equipment
Positive airway pressure delivery system
Non Electromedic Non Sterile
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