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SENSIGHT™ Extension Kit - Indonesia BPOM Medical Device Registration

SENSIGHT™ Extension Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31003220066. The device is manufactured by MEDTRONIC PUERTO RICO OPERATIONS CO., VILLALBA 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
SENSIGHT™ Extension Kit
Analysis ID: AKL 31003220066

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

Registration Date

Dec 21, 2022

Expiry Date

Jan 13, 2026

Product Type

Therapeutic Neurology Equipment

Implantable multi-programmable quadripolar deep brain stimulation system

Non Electromedic Sterile

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