CHIRANA AURA Basic - Indonesia BPOM Medical Device Registration
CHIRANA AURA Basic is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403916713. 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 PT. ALKESTRON SELF-SOURCE.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CHIRANA MEDICAL, A.SCountry of Origin
Slovakia
Authorized Representative
PT. ALKESTRON SELF-SOURCEAR Address
Komp Ruko Griya Inti Sentosa Jln. Griya Agung Blok O No. 95-96
Registration Date
Jul 04, 2022
Expiry Date
Apr 28, 2027
Product Type
Therapeutic Anesthesia Equipment
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