LITHO DK30 - Indonesia BPOM Medical Device Registration
LITHO DK30 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603323747. The device is manufactured by QUANTA SYSTEM S.P.A. from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. I-TECH LAFACOS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
QUANTA SYSTEM S.P.A.Country of Origin
Italy
Authorized Representative
PT. I-TECH LAFACOSAR Address
Gedung indra centra Blok M-N, Jl. Jendral suprapto No. 60, Kel Cempaka Putih barat , Kec. Cempaka Putih
Registration Date
Oct 03, 2024
Expiry Date
Dec 31, 2026
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
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