LASEMD Ultra - Indonesia BPOM Medical Device Registration
LASEMD Ultra is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603125903. The device is manufactured by LUTRONIC CORPORATION from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. PRIME MED INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LUTRONIC CORPORATIONCountry 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
Sep 22, 2021
Expiry Date
Jun 14, 2026
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
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