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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.

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BPOM Registered
Risk Class Kelas Resiko : C
NG Bio-Medicus Adult Arterial/Internal Jugular Cannula Kits
Analysis ID: AKL 20504120215

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Mexico

Authorized Representative

MEDTRONIC INDONESIA

AR 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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