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OMRON Electronic Nerve Stimulator - Indonesia BPOM Medical Device Registration

OMRON Electronic Nerve Stimulator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003220041. The device is manufactured by OMRON DALIAN CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. OMRON HEALTHCARE 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 : C
OMRON Electronic Nerve Stimulator
Analysis ID: AKL 21003220041

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. OMRON HEALTHCARE INDONESIA

AR Address

Menara Bidakara 1 Lt. 22 Jl. Gatot Subroto kav. 71-73 Jakarta Selatan.

Registration Date

Mar 09, 2023

Expiry Date

Jan 30, 2026

Product Type

Therapeutic Neurology Equipment

Transcutaneous electrical nerve stimulator for pain relief.

Non Radiation Electromedics

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