RADIFOCUS Angiographic Catheter - Indonesia BPOM Medical Device Registration
RADIFOCUS Angiographic Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501310687. The device is manufactured by TERUMO VIETNAM CO., LTD, from Vietnam, 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
TERUMO VIETNAM CO., LTD,Country of Origin
Vietnam
Authorized Representative
PT. TERUMO INDONESIAAR Address
Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta
Registration Date
Jul 04, 2022
Expiry Date
Apr 27, 2027
Product Type
Diagnostic Cardiology Equipment
Diagnostic intravascular catheter.
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