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KABEMA Patient Monitor - Indonesia BPOM Medical Device Registration

KABEMA Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502420244. The device is manufactured by SHENZHEN CREATIVE INDUSTRY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. WORK WITH YOU.

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BPOM Registered
Risk Class Kelas Resiko : B
KABEMA Patient Monitor
Analysis ID: AKL 20502420244

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. WORK WITH YOU

AR Address

KARYA BERSAMA ANDA

Registration Date

Jul 29, 2024

Expiry Date

Jul 25, 2027

Product Type

Monitoring Cardiology Equipment

Cardiac monitor (including cardiotachometer and rate alarm).

Non Radiation Electromedics

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