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RSHOCK Hi-TENS - Indonesia BPOM Medical Device Registration

RSHOCK Hi-TENS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003320152. The device is manufactured by WINBACK GO EAST CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ASA PRATAMA PARTNERS.

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
RSHOCK Hi-TENS
Analysis ID: AKL 21003320152

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Korea

Authorized Representative

PT. ASA PRATAMA PARTNERS

AR Address

MT Haryono Square No.OF 01/06 JL. MT.Haryono Kav.10, Kel. Bidara Cina , Kec. Jatinegara - Jakarta Timur

Registration Date

Aug 04, 2023

Expiry Date

Oct 31, 2025

Product Type

Therapeutic Neurology Equipment

Transcutaneous electrical nerve stimulator for pain relief.

Non Radiation Electromedics

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