LEONARDO Dual 200 - Indonesia BPOM Medical Device Registration
LEONARDO Dual 200 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603022698. The device is manufactured by CERAM OPTEC GMBH. from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. INDOMED KAHANASTI INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CERAM OPTEC GMBH.Country of Origin
Germany
Authorized Representative
PT. INDOMED KAHANASTI INDONESIAAR Address
Grand Centro Bintaro Blok B, Jalan Kodam Bintaro No.5A RT/RW.005/003 Kel. Pesanggrahan, Kec. Pesanggrahan, Jakarta Selatan. Telp. (021) 2270
Registration Date
Sep 20, 2022
Expiry Date
Jul 22, 2025
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
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