DR. LASER Summus Therapy Device - Indonesia BPOM Medical Device Registration
DR. LASER Summus Therapy Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403420341. The device is manufactured by WUHAN GUANGDUN TECHNOLOGY CO.,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is VERIMARK.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
WUHAN GUANGDUN TECHNOLOGY CO.,LTDCountry of Origin
China
Authorized Representative
VERIMARKAR Address
Komplek Roxy Mas Blok E2 No. 20 Jl. KH. Hasyim Ashari 125 Kel. Cideng Kec. Gambir Jakarta Pusat 10150
Registration Date
Sep 09, 2024
Expiry Date
Jun 20, 2029
Product Type
Therapeutic Physical Health Equipment
Infrared lamp.
Non Radiation Electromedics
