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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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Risk Class Kelas Resiko : C
CHIRANA AURA IN FAN

CHIRANA AURA V Ventilator

Analysis ID: AKL 20403321482

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Slovakia

Authorized Representative

ALKESTRON SELF-SOURCE

AR 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.

Non Radiation Electromedics

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