AIRFIT N30 - Indonesia BPOM Medical Device Registration
AIRFIT N30 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403126550. The device is manufactured by RESMED ASIA PTE LTD from Singapore, 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 ASIA PTE LTDCountry of Origin
Singapore
Authorized Representative
PT. QUALTEK CONSULTANT JAKARTAAR Address
Icon Business Park Blok K No 6, BSD City, Kab Tangerang, Banten
Registration Date
Nov 23, 2021
Expiry Date
Mar 31, 2025
Product Type
Therapeutic Anesthesia Equipment
Positive airway pressure delivery system
Non Electromedic Non Sterile
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