INJECTOMAT Lines PE - Indonesia BPOM Medical Device Registration
INJECTOMAT Lines PE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902413456. The device is manufactured by CLINICO MEDICAL SP. Z.O.O from Poland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FRESENIUS KABI INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CLINICO MEDICAL SP. Z.O.OCountry of Origin
Poland
Authorized Representative
PT. FRESENIUS KABI INDONESIAAR Address
Menara Bidakara 1 Lt.19, Jl. Gatot Subroto Kav 71 - 73 Menteng Dalam, Tebet, Jakarta Selatan 12870
Registration Date
Mar 09, 2023
Expiry Date
Sep 09, 2027
Product Type
Therapeutic General and Individual Hospital Equipment
Intravascular administration set.
Non Electromedic Sterile
INJECTOMAT Lines
FREKA Tube FR 8, 120cm, ENFit
VOLUMAT LINE Infusion Set VL ON 42
Freka Sil FR 16, ENFit
GRAVISET Bag, ENFit
VOLUMAT LINE Infusion Set VL ON 90
AMIKA Pump Set EasyBag, universal, ENPlus, ENFit
GRAVISET EasyBag, universal, ENPlus, ENFit
AMIKA Pump Set Bag, ENFit
APPLIX Pump Set Bag, ENFit
CONOX Pediatric Sensor
FRESENIUS KABI (NANCHANG) CO., LTD.
FRESENIUS KABI 3 Way Stopcock
FRESENIUS KABI (NANCHANG) CO., LTD.
FRESENIUS 3-Way-Stopcock
CLINICO MEDICAL SP. Z.O.O.
AMICUS Separator and Accessories
FRESENIUS KABI WARRENDALE.
VS 10 DEHP-Free
CLINICO MEDICAL SP. Z O.O.
AmiCORE Apheresis Kit - Single Needle with Two Platelet Containers and PAS Connector
FENWAL INTERNATIONAL, INC.
FRESENIUS Amicore Apheresis Kit - Single Needle
FENWAL INTERNATIONAL INC.
AGILIA SP PCA WIFI ID
FRESENIUS VIAL
AMICORE Apheresis Kit - Single Needle with Two Platelet Containers
FENWAL INTERNATIONAL INC.
COMPOLAB TM Cuvette
EKF-DIAGNOSTIC GMBH