SenSight™ Directional Lead Kit B33015 - Indonesia BPOM Medical Device Registration
SenSight™ Directional Lead Kit B33015 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31003220073. 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.
Risk Classification
Product Class
Kelas : 3
Manufacturer
MEDTRONIC PUERTO RICO OPERATIONS CO., VILLALBACountry of Origin
United States
Authorized Representative
MEDTRONIC INDONESIAAR Address
Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda
Registration Date
Nov 16, 2022
Expiry Date
Jan 13, 2026
Product Type
Therapeutic Neurology Equipment
Implantable multi-programmable quadripolar deep brain stimulation system
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