CAPIOX FX Advance - Indonesia BPOM Medical Device Registration
CAPIOX FX Advance is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504420035. The device is manufactured by ASHITAKA FACTORY OF TERUMO CORPORATION from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is TERUMO INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ASHITAKA FACTORY OF TERUMO CORPORATIONCountry of Origin
Japan
Authorized Representative
TERUMO INDONESIAAR Address
Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta
Registration Date
Mar 06, 2024
Expiry Date
Mar 14, 2028
Product Type
Surgical Cardiology Equipment
Cardiopulmonary bypass oxygenator.
Non Electromedic Sterile
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GLIDESHEATH SLENDER Hydrophilic Coated Introducer
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CAPIOX RX
ULTIMASTER Sirolimus Eluting Coronary Stent System
ULTIMASTER NAGOMI ™ Sirolimus Eluting Coronary Stent System
TR Band
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TERUMO TERUFUSION Infusion Pump TE-135
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TERUMO Digital Clinical Thermometer
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CHEMOSAFE LOCK™ Vented Vial Spike
ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V
CHEMOSAFE LOCK™ Universal Vented Vial Spike
ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V
5" (13 cm) Bag Spike Adapter w/CHEMOSAFE LOCK™ w/Red Cap, Vented Cap
ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V
TERUFUSION™ SS 10
SANMINA-SCI (SHENZHEN) LTD.
CHEMOSAFE LOCK™ Closed Vial Spike
ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V
CHEMOSAFE LOCK™
ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V
Glidesheath Slender
TERUMO VIETNAM CO., LTD.