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VENAR TS Anaesthesi Unit - Indonesia BPOM Medical Device Registration

VENAR TS Anaesthesi Unit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403710736. 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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BPOM Registered
Risk Class Kelas Resiko : C
VENAR TS Anaesthesi Unit
Analysis ID: AKL 20403710736

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Slovakia

Authorized Representative

PT. ALKESTRON SELF-SOURCE

AR Address

Komplek Ruko Griya Inti Sentosa, JI. Griya Agung Blok O No.95, RT.2/RW.20

Registration Date

Dec 13, 2024

Expiry Date

Sep 01, 2027

Product Type

Therapeutic Anesthesia Equipment

Gas machine for anesthesia or analgesia.

Non Radiation Electromedics

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