FUSION OASIS - One Action Stent Introduction System - Indonesia BPOM Medical Device Registration

FUSION OASIS - One Action Stent Introduction System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805320641. The device is manufactured by COOK IRELAND LTD. from Ireland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MURSMEDIC.

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.

Free Database

BPOM Registered

Risk Class Kelas Resiko : C

FUSION OASIS - One Action Stent Introduction System

Analysis ID: AKL 20805320641

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

COOK IRELAND LTD.

Country of Origin

Ireland

Authorized Representative

PT. MURSMEDIC

AR Address

The Kensington Office Tower Lantai 11, Jalan Boulevard Raya Nomor 1, Desa/Kelurahan Kelapa Gading Timur, Kec. Kelapa Gading, Kota Adm. Jakarta Utara, Provinsi DKI Jakarta, 14240