SKINREX HYDROMAGIC - Indonesia BPOM Medical Device Registration
SKINREX HYDROMAGIC is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11602810698. The device is manufactured by SKINREX CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. PRIME MED INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
SKINREX CO., LTD.Country of Origin
Korea
Authorized Representative
PT. PRIME MED INDONESIAAR Address
Gedung MT Haryono Square Lt. 3, Unit 03 /5B Jl. Otto Iskandardinata No. 390, Kel. Bidaracina, Kec. Jatinegara, Jakarta Timur 13330
Registration Date
Oct 19, 2020
Expiry Date
Oct 05, 2025
Product Type
Prosthetic Surgical Equipment
External facial fracture fixation appliance.
Non Radiation Electromedics
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