LUTRONIC GENIUS - Indonesia BPOM Medical Device Registration
LUTRONIC GENIUS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603023854. 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
Jul 14, 2020
Expiry Date
Feb 19, 2025
Product Type
Surgical Equipment
Electrosurgical cutting and coagulation device and accessories.
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