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.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
WEVER INSTRUMENTS CO.,LTD.Country of Origin
Korea
Authorized Representative
PT. SATYA ABADI VISIMEDAR 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.
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