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PROTEGE™ GPS™ Self-expanding Peripheral Stent System - Indonesia BPOM Medical Device Registration

PROTEGE™ GPS™ Self-expanding Peripheral Stent System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503420132. The device is manufactured by MEDTRONIC INC. (PLYMOUTH) from United States, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. 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 : D
PROTEGE™ GPS™ Self-expanding Peripheral Stent System
Analysis ID: AKL 30503420132

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

United States

Authorized Representative

PT. 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

Sep 20, 2024

Expiry Date

Feb 20, 2029

Product Type

Prosthetic Cardiology Equipment

Carotid Stent

Non Electromedic Sterile

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