SMARTXIDE Tetra Pro - Indonesia BPOM Medical Device Registration
SMARTXIDE Tetra Pro is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603422139. The device is manufactured by DEKA M.E.L.A S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. CEKINDO BUSINESS INTERNATIONAL.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DEKA M.E.L.A S.R.L.Country of Origin
Italy
Authorized Representative
PT. CEKINDO BUSINESS INTERNATIONALAR Address
CEKINDO BUSINESS INTERNATIONAL
Registration Date
Sep 12, 2024
Expiry Date
Apr 10, 2028
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
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