CELTRA PRESS - Indonesia BPOM Medical Device Registration
CELTRA PRESS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20605718795. The device is manufactured by DEGUDENT GMBH. from Germany, 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
DEGUDENT GMBH.Country of Origin
Germany
Authorized Representative
PT. DENTSPLY SIRONA INDONESIAAR Address
Gedung Tempo Scan Tower, Lantai 28, Jl. H.R. Rasuna Said Kav. 3-4
Registration Date
Oct 09, 2024
Expiry Date
Apr 01, 2026
Product Type
Other Dental Equipment
Porcelain powder for clinical use.
Non Electromedic Non Sterile
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