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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.

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BPOM Registered
Risk Class Kelas Resiko : C
NAVISEL Intravascular Guiding Catheter
Analysis ID: AKL 20501420221

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Korea

Authorized Representative

KIMERA FLUX INDONESIA

AR 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

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