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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 21003916698. 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 21003916698

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. OMRON HEALTHCARE INDONESIA

AR Address

MENARA BIDAKARA 2 LT 11 UNIT 1,2 DAN 3, JL. JEND. GATOT SUBROTO KAV. 71-73

Registration Date

Jun 21, 2024

Expiry Date

Dec 20, 2027

Product Type

Therapeutic Neurology Equipment

Transcutaneous electrical nerve stimulator for pain relief.

Non Radiation Electromedics

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