WISER 2 Diode Laser - Indonesia BPOM Medical Device Registration
WISER 2 Diode Laser is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603324812. The device is manufactured by LAMBDA SPA from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ANDAMAN MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LAMBDA SPACountry of Origin
Italy
Authorized Representative
PT. ANDAMAN MEDICAL INDONESIAAR Address
Menara Cardig Lantai 1, Jalan Raya Halim Perdanakusuma
Registration Date
Aug 28, 2023
Expiry Date
Jun 13, 2028
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
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