PRODEVICE Combo Pack Infusion Therapy - Safety - Indonesia BPOM Medical Device Registration
PRODEVICE Combo Pack Infusion Therapy - Safety is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902220012. The device is manufactured by GST CORPORATION LIMITED, INDIA; PT. BU KWANG MEDICAL, BANTEN; PT. ERACITA ASTAMIDA, DKI JAKARTA; SHANDONG DERMCOSY from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BETWEEN PARTNERS OF SELF-SUFFICIENCY.
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PRODEVICE Combo Pack Terapi Infus - Safety
Risk Classification
Product Class
Kelas : 2
Country of Origin
China
Authorized Representative
PT. BETWEEN PARTNERS OF SELF-SUFFICIENCYAR Address
Jl. Pos Pengumben Raya No.8 RT.005 RW.005, Sukabumi Selatan, Kebon Jeruk, Jakarta Barat 11560
Registration Date
Sep 26, 2022
Expiry Date
Oct 28, 2025
Product Type
Therapeutic General and Individual Hospital Equipment
Intravascular administration set
Non Electromedic Sterile
PRODEVICE Combo Pack Kateterisasi Urin A
HOSPITAL EQUIPMENT MANUFACTURING COMPANY; NINGBO GREATCARE MEDICAL MELALUI NINGBO GREATCARE TRADING; IDEAL MEDICAL MELALUI NINGBO GREETMED; YANGZHOU GOLDENWELL; CV. MULIA KASA; PT.PROSWEAL INDOMAX
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PRODEVICE Combo Pack Kateterisasi Urin B
HOSPITAL EQUIPMENT MANUFACTURING COMPANY; NINGBO GREATCARE MEDICAL MELALUI NINGBO GREATCARE TRADING; IDEAL MEDICAL MELALUI NINGBO GREETMED MEDICAL; YANGZHOU GOLDENWELL MEDICAL; CV. MULIA KASA
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