GO LASER - Indonesia BPOM Medical Device Registration
GO LASER is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403420069. The device is manufactured by HUBEI FITHOPE TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MULTI SHOP NUSANTARA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HUBEI FITHOPE TECHNOLOGY CO., LTD.Country of Origin
China
Authorized Representative
PT. MULTI SHOP NUSANTARAAR Address
The Bellezza Gapuraprima Office Tower Lantai 23 Unit 3, Jl. Letjend Soepeno No. 34, Arteri Permata Hijau, RT.005/RW.002, Kode Pos 12210, Desa/Kelurahan Grogol Utara, Kec. Kebayoran Lama, Kota Jakarta Selatan, Prov. DKI Jakarta
Registration Date
Feb 22, 2024
Expiry Date
Feb 20, 2027
Product Type
Therapeutic Physical Health Equipment
Infrared lamp.
Non Radiation Electromedics
