LAUNCHER Guiding Catheter - Indonesia BPOM Medical Device Registration
LAUNCHER Guiding Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501511139. The device is manufactured by MEDTRONIC VASCULAR from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is MEDTRONIC 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
MEDTRONIC VASCULARCountry of Origin
United States
Authorized Representative
MEDTRONIC INDONESIAAR Address
Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda, Desa/Kelurahan Kebayoran Lama Utara, Kec. Kebayoran Lama
Registration Date
Sep 13, 2023
Expiry Date
Feb 07, 2028
Product Type
Diagnostic Cardiology Equipment
Catheter guide wire.
Non Electromedic Sterile
NG BIO-MEDICUS Pediatric Venous Cannula and Introducers
MEDTRONIC MEXICO S DE R.L DE CV
NG Bio-Medicus Adult Arterial/Internal Jugular Cannula Kits
MEDTRONIC MEXICO S DE R.L DE CV
AFFINITY CP Centrifugal Blood Pump
MEDTRONIC MEXICO S. DE R.L. DE CV
MEDTRONIC Lumboperitonial Shunt
MEDTRONIC DOMINICANA (MANUFACTURA) S.A.
MEDTRONIC CSF Valves And Buttons
MEDTRONIC DOMINICANA (MANUFACTURA) S.A.
MEDTRONIC Ventricular Catheters
MEDTRONIC NEUROSURGERY
MEDTRONIC Shunt Accessories
MEDTRONIC DOMINICANA (MANUFACTURA) S.A.
MEDTRONIC Shunt Kits
MEDTRONIC DOMINICANA (MANUFACTURA) S.A.
MEDTRONIC EDM Lumbar
MEDTRONIC MEXICO S. DE R.L. DE CV
CG Future Sizer Sets
MEDTRONIC HEART VALVE DIVISION

