CAPIOX FX - Indonesia BPOM Medical Device Registration
CAPIOX FX is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504905281. 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 PT. TERUMO INDONESIA.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Manufacturer
ASHITAKA FACTORY Of TERUMO CORPORATIONCountry of Origin
Japan
Authorized Representative
PT. TERUMO INDONESIAAR Address
Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta
Registration Date
Dec 28, 2022
Expiry Date
Apr 19, 2027
Product Type
Surgical Cardiology Equipment
Cardiopulmonary bypass oxygenator.
Non Electromedic Sterile
TERUMO TERUFUSION Infusion Pump TE-172
ASHITAKA FACTORY OF TERUMO CORPORATION.
REVEOS Automated Blood Processing System And Accessories
TERUMO BCT INC.
MEDISAFE FIT Smile Blood Glucose Meter
TERUMO CORPORATION.
MEDICA EO Hemoconcentrator
MEDICA S.P.A.
RADIFOCUS Glidewire Advantage
ASHITAKA FACTORY OF TERUMO CORPORATION JAPAN
SURSHIELD SURFLO II
KOFU FACTORY OF TERUMO CORPORATION
CHEMOSAFE LOCK™ Vented Vial Spike, 20mm
ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.
TERUFUSION™ SS 10
SANMINA-SCI (SHENZHEN) LTD.
CHEMOSAFE LOCK™ Bag Spike
ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.
Trima Accel® LRS® Platelet, Plasma Set
TFB MANUFACTURING SRL