NG Bio-Medicus Adult Arterial/Internal Jugular Cannula Kits - Indonesia BPOM Medical Device Registration
NG Bio-Medicus Adult Arterial/Internal Jugular Cannula Kits is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504120215. The device is manufactured by MEDTRONIC MEXICO S DE R.L DE CV from Mexico, 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 MEXICO S DE R.L DE CVCountry of Origin
Mexico
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
Feb 11, 2025
Expiry Date
Feb 20, 2029
Product Type
Surgical Cardiology Equipment
Cardiopulmonary bypass vascular catheter, cannula, or tubing.
Non Electromedic Sterile
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