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CHIRANA AURA Ventilator - Indonesia BPOM Medical Device Registration

CHIRANA AURA Ventilator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403713556. 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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BPOM Registered
Risk Class Kelas Resiko : C
CHIRANA AURA Ventilator
Analysis ID: AKL 20403713556

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

Jul 19, 2022

Expiry Date

Apr 28, 2027

Product Type

Therapeutic Anesthesia Equipment

Continuous ventilator.

Non Radiation Electromedics

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