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DBS Lead Kit for Deep Brain Stimulation - Indonesia BPOM Medical Device Registration

DBS Lead Kit for Deep Brain Stimulation is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31003513814. 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 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
DBS Lead Kit for Deep Brain Stimulation
Analysis ID: AKL 31003513814

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

United States

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

Jan 22, 2024

Expiry Date

Feb 07, 2028

Product Type

Therapeutic Neurology Equipment

Implantable multi-programmable quadripolar deep brain stimulation system

Non Electromedic Non Sterile

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