SMARTLITE PRO ENDOACTIVATOR™ - Indonesia BPOM Medical Device Registration
SMARTLITE PRO ENDOACTIVATOR™ is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20603420010. The device is manufactured by DENTSPLY LLC from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DENTSPLY SIRONA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DENTSPLY LLCCountry of Origin
United States
Authorized Representative
PT. DENTSPLY SIRONA INDONESIAAR Address
Gedung Tempo Scan Tower, Lantai 28, Jl. H.R. Rasuna Said Kav. 3-4
Registration Date
Jan 12, 2024
Expiry Date
Jan 05, 2028
Product Type
Surgical Dental Equipment
Dental handpiece and accessories
Non Radiation Electromedics
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