KABEMA Infusion Pump - Indonesia BPOM Medical Device Registration
KABEMA Infusion Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902420795. 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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Risk Classification
Product Class
Kelas : 2
Manufacturer
SHENZHEN HAWK MEDICAL INSTRUMENT CO., LTD.Country of Origin
China
Authorized Representative
PT. WORK WITH YOUAR Address
KARYA BERSAMA ANDA
Registration Date
Aug 04, 2024
Expiry Date
Aug 02, 2027
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
Non Radiation Electromedics
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