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 20902420911. The device is manufactured by ZHEJIANG MDKINGDOM TECHNOLOGY 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
ZHEJIANG MDKINGDOM TECHNOLOGY CO., LTD.Country of Origin
China
Authorized Representative
PT. WORK WITH YOUAR Address
KARYA BERSAMA ANDA
Registration Date
Aug 28, 2024
Expiry Date
May 04, 2026
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
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