PRODEVICE Combo Pack Blood Set - Indonesia BPOM Medical Device Registration
PRODEVICE Combo Pack Blood Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902322511. The device is manufactured by G.S.T CORPORATION LIMITED ; PT. ERACHITA ASTAMIDA ; 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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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 05, 2023
Expiry Date
Sep 04, 2026
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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