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WEVER Extracorporeal Shock Wave Treatment System - Indonesia BPOM Medical Device Registration

WEVER Extracorporeal Shock Wave Treatment System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403320861. The device is manufactured by WEVER INSTRUMENTS CO.,LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SATYA ABADI VISIMED.

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
WEVER Extracorporeal Shock Wave Treatment System
Analysis ID: AKL 21403320861

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Korea

Authorized Representative

PT. SATYA ABADI VISIMED

AR Address

Ruko Sentra Menteng Blok MN-28 Bintaro Jaya Sektor 7 Pondok Jaya Pondok Aren Tangerang 15224

Registration Date

Nov 24, 2023

Expiry Date

Mar 30, 2028

Product Type

Therapeutic Physical Health Equipment

Shortwave diathermy.

Non Radiation Electromedics

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