NAVISEL Intravascular Guiding Catheter - Indonesia BPOM Medical Device Registration
NAVISEL Intravascular Guiding Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501420221. The device is manufactured by SEAWON MEDITECH CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is KIMERA FLUX 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
SEAWON MEDITECH CO., LTD.Country of Origin
Korea
Authorized Representative
KIMERA FLUX INDONESIAAR Address
Ruko Melati Vista V21/A2 Jl.Boulevard
Registration Date
Apr 18, 2024
Expiry Date
Jan 24, 2026
Product Type
Diagnostic Cardiology Equipment
Percutaneous catheter.
Non Electromedic Sterile

