CHIRANA AURA IN FAN - Indonesia BPOM Medical Device Registration
CHIRANA AURA IN FAN is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403321482. The device is manufactured by CHIRANA MEDICAL, A.S from Slovakia, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is ALKESTRON SELF-SOURCE.
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CHIRANA AURA V Ventilator
Risk Classification
Product Class
Kelas : 2
Manufacturer
CHIRANA MEDICAL, A.SCountry of Origin
Slovakia
Authorized Representative
ALKESTRON SELF-SOURCEAR Address
Komp Ruko Griya Inti Sentosa Jln. Griya Agung Blok O No. 95-96
Registration Date
Aug 09, 2023
Expiry Date
Sep 01, 2027
Product Type
Therapeutic Anesthesia Equipment
Continuous ventilator.
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