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KABEMA Syringe Pump - Indonesia BPOM Medical Device Registration

KABEMA Syringe Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902420673. The device is manufactured by SHENZHEN HAWK MEDICAL INSTRUMENT 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 Syringe Pump
Analysis ID: AKL 20902420673

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 02, 2024

Expiry Date

Jul 02, 2027

Product Type

Therapeutic General and Individual Hospital Equipment

Infusion pump.

Non Radiation Electromedics

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