COOPDECH® Balloonjector® - Indonesia BPOM Medical Device Registration
COOPDECH® Balloonjector® is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902311960. The device is manufactured by DAIKEN MEDICAL CO., LTD. from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BRIDGE TWO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DAIKEN MEDICAL CO., LTD.Country of Origin
Japan
Authorized Representative
PT. BRIDGE TWOAR Address
Jl. Petojo Melintang No. 17
Registration Date
Apr 23, 2024
Expiry Date
Jan 12, 2029
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
Non Electromedic Sterile
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