AIRBLEND Heated Humidifier System - Indonesia BPOM Medical Device Registration
AIRBLEND Heated Humidifier System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403126703. The device is manufactured by AIRBLEND MEDICAL DEVICE MANUFACTURING INC from Turkey, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FA ANTARES MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
AIRBLEND MEDICAL DEVICE MANUFACTURING INCCountry of Origin
Turkey
Authorized Representative
PT. FA ANTARES MEDIKAAR Address
Ruko Golden Boulevard Blok i No 7 BSD City
Registration Date
Nov 08, 2021
Expiry Date
May 31, 2024
Product Type
Therapeutic Anesthesia Equipment
High flow humidified oxygen delivery device.
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