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MEDTRONIC External Neustimulator - Indonesia BPOM Medical Device Registration

MEDTRONIC External Neustimulator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003712261. The device is manufactured by MEDTRONIC NEUROMODULATION. from United States, and is classified as Risk Class Kelas Resiko : B. 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 : B
MEDTRONIC External Neustimulator
Analysis ID: AKL 21003712261

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

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

Nov 12, 2020

Expiry Date

Mar 11, 2025

Product Type

Therapeutic Neurology Equipment

Implanted spinal cord stimulator for pain relief.

Non Radiation Electromedics

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